Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562012617
rs1562012617
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type
T 0.700 CausalMutation CLINVAR