POMC, proopiomelanocortin, 5443

N. diseases: 873; N. variants: 39
Disease: Proopiomelanocortin Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918111
rs121918111
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918112
rs121918112
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1553400259
rs1553400259
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		G 0.700 CausalMutation CLINVAR
dbSNP: rs753856820
rs753856820
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		T 0.700 CausalMutation CLINVAR
dbSNP: rs796065034
rs796065034
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		C 0.700 CausalMutation CLINVAR
dbSNP: rs796065035
rs796065035
Entrez Id: 5443
Gene Symbol: POMC
POMC
CUI: C1857854
Disease:
Proopiomelanocortin Deficiency 		GCC 0.700 CausalMutation CLINVAR