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: rs137852804
rs137852804
CHRNA1
1 1.000 2 174750035 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 3 1999 2004
dbSNP: rs137852805
rs137852805
CHRNA1
1 1.000 2 174753524 missense variant A/C snv 4.0E-06 0.800 1.000 3 1999 2004
dbSNP: rs137852806
rs137852806
CHRNA1
1 1.000 2 174750122 missense variant A/G snv 0.800 1.000 3 1999 2004
dbSNP: rs137852807
rs137852807
CHRNA1
1 1.000 2 174754305 missense variant C/G;T snv 1.6E-05 0.800 1.000 3 1999 2004
dbSNP: rs483353045
rs483353045
CHRNE ; C17orf107
1 1.000 17 4902011 missense variant G/T snv 0.700 0