Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs775081992
rs775081992
Entrez Id: 27241
Gene Symbol: BBS9
BBS9
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency
T 0.700 CausalMutation CLINVAR
dbSNP: rs886039799
rs886039799
Entrez Id: 27241
Gene Symbol: BBS9
BBS9
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency
A 0.700 CausalMutation CLINVAR
dbSNP: rs886039801
rs886039801
Entrez Id: 27241
Gene Symbol: BBS9
BBS9
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency
A 0.700 CausalMutation CLINVAR