HCCS, holocytochrome c synthase, 3052

N. diseases: 135; N. variants: 4
Disease: MICROPHTHALMIA, SYNDROMIC 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917888
rs121917888
Entrez Id: 395;3052
Gene Symbol: ARHGAP6;HCCS
ARHGAP6;HCCS
CUI: C0796070
Disease:
MICROPHTHALMIA, SYNDROMIC 7 		T 0.700 CausalMutation CLINVAR