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: rs121917927
rs121917927
2 0.925 0.040 2 166046969 missense variant C/G;T snv 0.800 1.000 32 2003 2017
dbSNP: rs121917971
rs121917971
4 0.851 0.080 2 166037885 missense variant C/G;T snv 0.800 1.000 31 2003 2017
dbSNP: rs121917918
rs121917918
4 0.851 0.040 2 166058651 missense variant C/A;T snv 0.800 1.000 25 2003 2017
dbSNP: rs121918775
rs121918775
5 0.827 0.080 2 166037886 missense variant G/A;T snv 0.800 1.000 25 2003 2017
dbSNP: rs121918733
rs121918733
1 1.000 0.040 2 166058684 missense variant A/G snv 0.800 1.000 24 2003 2017
dbSNP: rs121918791
rs121918791
3 0.882 0.080 2 165992333 missense variant G/A snv 0.800 1.000 24 2002 2017
dbSNP: rs121917921
rs121917921
3 0.882 0.040 2 165991927 missense variant G/A snv 0.800 1.000 22 2003 2017
dbSNP: rs121917922
rs121917922
1 1.000 0.040 2 165992302 missense variant G/A;C snv 0.800 1.000 22 2003 2017
dbSNP: rs121917923
rs121917923
1 1.000 0.040 2 166047725 missense variant G/A;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917937
rs121917937
2 0.925 0.040 2 166052866 missense variant A/C snv 0.800 1.000 22 2003 2017
dbSNP: rs121917938
rs121917938
1 1.000 0.040 2 166051845 missense variant A/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121917960
rs121917960
1 1.000 0.040 2 166002753 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917965
rs121917965
1 1.000 0.040 2 166058652 missense variant G/A snv 0.800 1.000 22 2003 2017
dbSNP: rs121917976
rs121917976
3 0.882 0.080 2 165992341 missense variant C/G;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917980
rs121917980
1 1.000 0.040 2 165991928 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917985
rs121917985
1 1.000 0.040 2 166051968 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917986
rs121917986
3 0.882 0.040 2 166002588 missense variant C/G;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917990
rs121917990
1 1.000 0.040 2 166043836 missense variant T/A;C snv 0.800 1.000 22 2003 2017
dbSNP: rs121918735
rs121918735
2 1.000 0.040 2 166051906 missense variant G/A;T snv 3.2E-05 0.800 1.000 22 2003 2017
dbSNP: rs121918736
rs121918736
2 1.000 0.040 2 166037907 missense variant G/A;C snv 0.800 1.000 22 2003 2017
dbSNP: rs121918737
rs121918737
1 1.000 0.040 2 166037868 missense variant A/C snv 0.800 1.000 22 2003 2017
dbSNP: rs121918738
rs121918738
1 1.000 0.040 2 166013820 missense variant G/A;T snv 1.6E-05 0.800 1.000 22 2003 2017
dbSNP: rs121918739
rs121918739
1 1.000 0.040 2 166012210 missense variant T/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121918740
rs121918740
1 1.000 0.040 2 166012128 missense variant A/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121918741
rs121918741
1 1.000 0.040 2 165999763 missense variant C/T snv 0.800 1.000 22 2003 2017