Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906265
rs387906265
Entrez Id: 114625
Gene Symbol: ERMAP
ERMAP
CUI: C4017180
Disease:
SCIANNA BLOOD GROUP SYSTEM, SC:-1,-2 PHENOTYPE 		T 0.700 CausalMutation CLINVAR
dbSNP: rs56136737
rs56136737
Entrez Id: 114625
Gene Symbol: ERMAP
ERMAP
CUI: C1862204
Disease:
RADIN BLOOD GROUP ANTIGEN 		G 0.700 GeneticVariation CLINVAR