Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35983258
rs35983258
Entrez Id: 3047
Gene Symbol: HBG1
HBG1
CUI: C1841621
Disease:
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
A 0.700 CausalMutation CLINVAR