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: rs781784543
rs781784543
1 1.000 0.080 11 119026979 stop gained G/A snv 2.4E-05 0.700 1.000 6 1998 2014
dbSNP: rs121908976
rs121908976
2 0.925 0.080 11 119028288 stop gained C/T snv 8.4E-06 0.700 1.000 4 1998 2005
dbSNP: rs551439289
rs551439289
1 1.000 0.080 11 119027069 stop gained G/A snv 8.1E-06 7.0E-06 0.700 1.000 3 1998 2010
dbSNP: rs121908975
rs121908975
1 1.000 0.080 11 119025251 stop gained C/A;T snv 1.2E-05 0.700 0
dbSNP: rs121908979
rs121908979
1 1.000 0.080 11 119024957 stop gained G/A;T snv 4.4E-05 0.700 0
dbSNP: rs1444468055
rs1444468055
1 1.000 0.080 11 119029260 stop gained G/T snv 1.2E-05 0.700 0
dbSNP: rs121908978
rs121908978
1 1.000 0.080 11 119029287 missense variant C/T snv 1.2E-05 0.800 1.000 29 1997 2017
dbSNP: rs193302900
rs193302900
1 1.000 0.080 11 119026640 missense variant A/T snv 7.0E-06 0.800 1.000 24 1997 2011
dbSNP: rs80356490
rs80356490
1 1.000 0.080 11 119025299 missense variant C/A snv 7.8E-05 7.7E-05 0.800 1.000 24 1997 2014
dbSNP: rs80356489
rs80356489
3 0.882 0.200 11 119028223 missense variant A/G snv 7.0E-06 0.810 1.000 21 1997 2014
dbSNP: rs80356492
rs80356492
1 1.000 0.080 11 119025215 missense variant C/T snv 5.6E-05 2.1E-05 0.700 1.000 21 1997 2014
dbSNP: rs121908980
rs121908980
1 1.000 0.080 11 119025298 missense variant C/T snv 0.800 1.000 20 1997 2011
dbSNP: rs193302901
rs193302901
1 1.000 0.080 11 119025196 missense variant G/C;T snv 4.0E-06; 4.0E-06 0.700 1.000 20 1997 2011
dbSNP: rs193302902
rs193302902
1 1.000 0.080 11 119027035 missense variant A/G snv 7.0E-06 0.700 1.000 20 1997 2011
dbSNP: rs193302903
rs193302903
1 1.000 0.080 11 119026052 missense variant C/T snv 0.700 1.000 20 1997 2011
dbSNP: rs193302882
rs193302882
1 1.000 0.080 11 119029288 missense variant G/A snv 4.0E-06 1.4E-05 0.800 1.000 8 1998 2014
dbSNP: rs193302881
rs193302881
1 1.000 0.080 11 119029311 missense variant C/G;T snv 1.6E-05 1.4E-05 0.800 1.000 5 1998 2014
dbSNP: rs193302888
rs193302888
1 1.000 0.080 11 119027681 missense variant G/A snv 0.800 1.000 5 2000 2008
dbSNP: rs193302883
rs193302883
1 1.000 0.080 11 119027806 missense variant C/T snv 1.4E-05 0.800 1.000 3 2002 2014
dbSNP: rs193302887
rs193302887
2 1.000 0.080 11 119029300 missense variant A/G snv 0.800 1.000 2 2002 2008
dbSNP: rs193302878
rs193302878
1 1.000 0.080 11 119026985 missense variant A/G snv 0.710 1.000 1 2009 2009
dbSNP: rs193302880
rs193302880
1 1.000 0.080 11 119026053 missense variant G/A snv 1.3E-05 0.700 1.000 1 2014 2014
dbSNP: rs193302885
rs193302885
1 1.000 0.080 11 119028373 missense variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs193302886
rs193302886
1 1.000 0.080 11 119028312 missense variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs80356482
rs80356482
5 0.851 0.160 17 42909418 missense variant G/A;C snv 1.6E-05; 5.2E-05 0.010 1.000 1 2002 2002