CRH, corticotropin releasing hormone, 1392

N. diseases: 402; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12721510
rs12721510 		1.000 0.080 8 66178947 upstream gene variant G/T snv 4.3E-02
CUI: C1835905
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 4
Epilepsy, Nocturnal Frontal Lobe, Type 4 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2005 2005
dbSNP: rs72556399
rs72556399 		1.000 0.080 8 66178643 upstream gene variant C/G snv 2.0E-04
CUI: C1835905
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 4
Epilepsy, Nocturnal Frontal Lobe, Type 4 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2005 2005