Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918111
rs121918111
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121918112
rs121918112
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1553400259
rs1553400259
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		G 0.700 CausalMutation CLINVAR

dbSNP: rs28932472
rs28932472
POMC
CUI: C4016341
Disease: OBESITY, EARLY-ONSET, SUSCEPTIBILITY TO
OBESITY, EARLY-ONSET, SUSCEPTIBILITY TO 		C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs753856820
rs753856820
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		T 0.700 CausalMutation CLINVAR

dbSNP: rs796065034
rs796065034
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		C 0.700 CausalMutation CLINVAR

dbSNP: rs796065035
rs796065035
POMC
CUI: C1857854
Disease: Proopiomelanocortin Deficiency
Proopiomelanocortin Deficiency 		GCC 0.700 CausalMutation CLINVAR