SCO2, synthesis of cytochrome C oxidase 2, 9997

N. diseases: 6; N. variants: 58
Disease: MYOPIA 6 (disorder) ×
Source: CLINVAR ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315511
rs74315511
Entrez Id: 9997;29781
Gene Symbol: SCO2;NCAPH2
SCO2;NCAPH2
CUI: C1837148
Disease:
MYOPIA 6 (disorder) 		T 0.800 CausalMutation CLINVAR
dbSNP: rs74315510
rs74315510
Entrez Id: 9997;29781
Gene Symbol: SCO2;NCAPH2
SCO2;NCAPH2
CUI: C1837148
Disease:
MYOPIA 6 (disorder) 		A 0.700 CausalMutation CLINVAR