CRH, corticotropin releasing hormone, 1392

N. diseases: 402; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12721510
rs12721510
Entrez Id: 1392
Gene Symbol: CRH
CRH
CUI: C1835905
Disease:
Epilepsy, Nocturnal Frontal Lobe, Type 4 		T 0.700 CausalMutation CLINVAR Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene. 16222669 2005
dbSNP: rs72556399
rs72556399
Entrez Id: 1392
Gene Symbol: CRH
CRH
CUI: C1835905
Disease:
Epilepsy, Nocturnal Frontal Lobe, Type 4 		G 0.700 CausalMutation CLINVAR Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene. 16222669 2005