C1842090[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3068127	NM_001001548.3(CD36):c.107del (p.Lys36fs)	CD36 (K36fs)	Deletion (frameshift variant +3 more)	Platelet-type bleeding disorder 10	GLikely pathogenic
Select item 417962	NM_001001548.3(CD36):c.429+2T>C	CD36	Single nucleotide variant (splice donor variant)	Platelet-type bleeding disorder 10 +2 more	GConflicting classifications of pathogenicity
Select item 3065787	NM_001001548.3(CD36):c.588del (p.Thr197fs)	CD36 (T121fs +3 more)	Deletion (frameshift variant +2 more)	Platelet-type bleeding disorder 10	GLikely pathogenic
Select item 632507	NM_001001548.3(CD36):c.1079T>G (p.Leu360Ter)	CD36 (L360* +5 more)	Single nucleotide variant (nonsense +1 more)	Platelet-type bleeding disorder 10 +1 more	GConflicting classifications of pathogenicity
Select item 3065439	NM_001001548.3(CD36):c.1206_1230dup (p.Val411fs)	CD36 (V411fs +5 more)	Duplication (frameshift variant +1 more)	Platelet-type bleeding disorder 10	GLikely pathogenic
Select item 1324033	NM_001001548.3(CD36):c.1240_1243dup (p.Trp415fs)	CD36 (W260fs +5 more)	Duplication (frameshift variant +1 more)	Platelet-type bleeding disorder 10	GPathogenic/Likely pathogenic
Select item 3067875	NM_001001548.3(CD36):c.1345_1348del (p.Leu449fs)	CD36 (L294fs +5 more)	Deletion (frameshift variant +1 more)	Platelet-type bleeding disorder 10	GUncertain significance

ClinVar