Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606726
rs267606726
Entrez Id: 1146
Gene Symbol: CHRNG
CHRNG
CUI: C1854678
Disease:
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE
G 0.800 CausalMutation CLINVAR
dbSNP: rs267606726
rs267606726
Entrez Id: 1146
Gene Symbol: CHRNG
CHRNG
CUI: C1854678
Disease:
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE
0.800 GeneticVariation UNIPROT