| | LOC121740684, LOC121740685 +4735 more | Copy number loss | See cases | |
| | ABHD11, ABHD11-AS1 +317 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | CACNA2D1, CACNA2D1-AS1 +79 more | Deletion | Seizure +1 more | |
| | | Single nucleotide variant | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (intron variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (intron variant +1 more) | Coronary heart disease, susceptibility to, 7 | |
| | | Single nucleotide variant (intron variant) | Type 2 diabetes mellitus | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Deletion (frameshift variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (splice donor variant +1 more) | Stroke disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (intron variant) | CD36-related disorder | |
| | | Microsatellite (intron variant) | Platelet-type bleeding disorder 10 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Deletion (frameshift variant +3 more) | not provided | |
| | | Indel (frameshift variant +3 more) | CD36-related disorder | |
| | | Single nucleotide variant (missense variant +3 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (nonsense +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (nonsense +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (nonsense +3 more) | Platelet-type bleeding disorder 10 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +3 more) | Inherited bleeding disorder, platelet-type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (intron variant) | Type 2 diabetes mellitus | |
| | | Single nucleotide variant (intron variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Microsatellite (frameshift variant +2 more) | Platelet-type bleeding disorder 10 +2 more | |
| | | Microsatellite (frameshift variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Duplication (frameshift variant +2 more) | CD36-related disorder | |
| | | Duplication (inframe_insertion +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (nonsense +2 more) | Platelet-type bleeding disorder 10 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | CD36-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (splice donor variant) | Platelet-type bleeding disorder 10 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (intron variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Platelet-type bleeding disorder 10 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +3 more) | CD36-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +3 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +3 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Deletion (frameshift variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | CD36-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | CD36-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Deletion (frameshift variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (synonymous variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +2 more) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (splice donor variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Platelet-type bleeding disorder 10 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Platelet-type bleeding disorder 10 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |