Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34690599
rs34690599
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C4693822
Disease:
ERYTHROCYTOSIS, FAMILIAL, 6
C 0.700 CausalMutation CLINVAR