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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
C1QTNF5, MFRP
(S338R)
Single nucleotide variant
(5 prime UTR variant +1 more)
MFRP-related disorder
+4 more
GConflicting classifications of pathogenicity
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
+3 more
GConflicting classifications of pathogenicity
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
+3 more
GBenign/Likely benign
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