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: rs137852798
rs137852798
CHRNA1
1 1.000 2 174753570 missense variant G/A;C;T snv 1.6E-05 0.800 1.000 5 1995 2006
dbSNP: rs137852799
rs137852799
CHRNA1
1 1.000 2 174754233 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.0E-05 0.800 1.000 5 1995 2006
dbSNP: rs137852800
rs137852800
CHRNA1
1 1.000 2 174750127 missense variant G/A snv 0.800 1.000 5 1995 2006
dbSNP: rs137852801
rs137852801
CHRNA1
2 0.925 0.120 2 174754242 missense variant C/T snv 0.800 1.000 5 1995 2006
dbSNP: rs137852802
rs137852802
CHRNA1
1 1.000 2 174750082 missense variant C/A snv 0.800 1.000 5 1995 2006
dbSNP: rs137852803
rs137852803
CHRNA1
2 1.000 2 174750143 missense variant C/A;G;T snv 2.8E-05; 4.0E-06; 8.0E-06 0.800 1.000 5 1995 2006
dbSNP: rs137852808
rs137852808
CHRNA1
1 1.000 2 174748184 missense variant G/A;C snv 8.0E-06 0.800 1.000 5 1995 2006
dbSNP: rs483353046
rs483353046
CHRNA1
1 1.000 2 174753544 missense variant G/A;T snv 0.700 0