rs281865071, CHRNB2

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Epilepsy, Nocturnal Frontal Lobe, Type 4
CUI: C1835905
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 4
11 0.882 0.080 1 154571759 missense variant C/G;T snv 0.700 0
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.882 0.080 1 154571759 missense variant C/G;T snv 0.020 1.000 2 2005 2008
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
CUI: C3696898
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
8 0.882 0.080 1 154571759 missense variant C/G;T snv 0.010 1.000 1 2008 2008
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.882 0.080 1 154571759 missense variant C/G;T snv 0.010 1.000 1 2005 2005
Forgetful
CUI: C0542476
Disease: Forgetful
18 0.882 0.080 1 154571759 missense variant C/G;T snv 0.010 1.000 1 2008 2008