Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894063
rs104894063
CHRNA2
3 0.882 0.120 8 27463607 missense variant A/T snv 0.800 1.000 1 2006 2006
dbSNP: rs1018084204
rs1018084204
CHRNA2
2 0.925 0.080 8 27463317 missense variant G/A snv 4.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs12721510
rs12721510
CRH
1 1.000 0.080 8 66178947 upstream gene variant G/T snv 4.3E-02 0.700 1.000 1 2005 2005
dbSNP: rs72556399
rs72556399
CRH
1 1.000 0.080 8 66178643 upstream gene variant C/G snv 2.0E-04 0.700 1.000 1 2005 2005
dbSNP: rs121909580
rs121909580
CHRNA4
3 0.882 0.080 20 63350572 missense variant G/A;C snv 0.700 0
dbSNP: rs1554514507
rs1554514507
CHRNA2
1 1.000 0.080 8 27463554 missense variant T/A snv 0.700 0
dbSNP: rs281865066
rs281865066
CHRNA4
1 1.000 0.080 20 63350533 missense variant G/A snv 0.700 0
dbSNP: rs281865069
rs281865069
CHRNB2
1 1.000 0.080 1 154571724 missense variant C/G snv 0.700 0
dbSNP: rs281865070
rs281865070
CHRNB2
1 1.000 0.080 1 154571746 missense variant T/C snv 0.700 0
dbSNP: rs281865071
rs281865071
CHRNB2
5 0.882 0.080 1 154571759 missense variant C/G;T snv 0.700 0
dbSNP: rs74315291
rs74315291
CHRNB2
3 0.882 0.080 1 154571682 missense variant G/A;C;T snv 0.700 0