Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893801
rs104893801
Entrez Id: 6657;347689
Gene Symbol: SOX2;SOX2-OT
SOX2;SOX2-OT
CUI: C1859773
Disease:
Microphthalmia, Syndromic 3
A 0.700 CausalMutation CLINVAR