KLHL29, kelch like family member 29, 114818

N. diseases: 15; N. variants: 12
Disease: Epilepsy, Generalized ×
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: rs4665630
rs4665630 		0.925 0.080 2 23675447 intron variant C/T snv 0.78
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.700 1.000 1 2018 2018