Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4225188
Disease:
MEIER-GORLIN SYNDROME 6
T 0.700 CausalMutation CLINVAR