COX7B, cytochrome c oxidase subunit 7B, 1349

N. diseases: 104; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514583
rs397514583
Entrez Id: 1349
Gene Symbol: COX7B
COX7B
CUI: C3550921
Disease:
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2 		A 0.700 CausalMutation CLINVAR
dbSNP: rs397514584
rs397514584
Entrez Id: 1349
Gene Symbol: COX7B
COX7B
CUI: C3550921
Disease:
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2 		G 0.700 CausalMutation CLINVAR
dbSNP: rs397514585
rs397514585
Entrez Id: 1349
Gene Symbol: COX7B
COX7B
CUI: C3550921
Disease:
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2 		T 0.700 CausalMutation CLINVAR