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: rs137852973
rs137852973
13 0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 0.710 1.000 7 2004 2016
dbSNP: rs879253777
rs879253777
2 0.925 0.080 1 11999009 missense variant G/A;T snv 0.710 1.000 5 2005 2016
dbSNP: rs879254011
rs879254011
1 1.000 0.080 1 12002034 missense variant G/A;C snv 0.700 1.000 15 2006 2017
dbSNP: rs56984562
rs56984562
6 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.700 1.000 14 2003 2017
dbSNP: rs137852972
rs137852972
10 0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 0.700 1.000 12 2004 2015
dbSNP: rs863224069
rs863224069
1 1.000 0.080 1 11996158 missense variant C/T snv 0.700 1.000 12 2004 2016
dbSNP: rs119103268
rs119103268
6 0.827 0.080 1 11992689 missense variant C/T snv 0.700 1.000 11 2008 2015
dbSNP: rs1553265342
rs1553265342
1 1.000 0.080 1 156134909 missense variant GC/TT mnv 0.700 1.000 11 2000 2015
dbSNP: rs28940291
rs28940291
9 0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 0.700 1.000 11 2004 2014
dbSNP: rs61672878
rs61672878
11 0.776 0.200 1 156136094 missense variant G/A;T snv 0.700 1.000 11 2000 2016
dbSNP: rs119103263
rs119103263
19 0.827 0.240 1 11992659 missense variant C/T snv 0.700 1.000 10 2004 2016
dbSNP: rs119103265
rs119103265
5 0.827 0.120 1 12002033 missense variant C/T snv 0.700 1.000 10 2006 2017
dbSNP: rs267607599
rs267607599
2 0.925 0.120 1 156136422 missense variant A/G;T snv 0.700 1.000 10 2000 2015
dbSNP: rs57520892
rs57520892
8 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 0.700 1.000 10 1999 2015
dbSNP: rs119103267
rs119103267
7 0.790 0.160 1 12009641 missense variant C/T snv 2.5E-04 2.8E-04 0.700 1.000 9 1976 2017
dbSNP: rs267607555
rs267607555
6 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 9 2004 2017
dbSNP: rs397517889
rs397517889
3 0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 0.700 1.000 9 2003 2014
dbSNP: rs58596362
rs58596362
7 0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 0.700 1.000 9 2003 2017
dbSNP: rs755065651
rs755065651
1 1.000 0.080 1 11999055 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.700 1.000 9 2009 2016
dbSNP: rs863224967
rs863224967
1 1.000 0.080 1 12002069 missense variant A/G;T snv 4.0E-06 0.700 1.000 9 2006 2017
dbSNP: rs121912496
rs121912496
3 0.882 0.120 1 156134910 missense variant C/G;T snv 0.700 1.000 8 2008 2015
dbSNP: rs1553142428
rs1553142428
1 1.000 0.080 1 11996157 missense variant A/G snv 0.700 1.000 8 2004 2014
dbSNP: rs59026483
rs59026483
7 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.700 1.000 8 2002 2015
dbSNP: rs60458016
rs60458016
5 0.827 0.120 1 156136036 stop gained G/A;T snv 0.700 1.000 8 2000 2014
dbSNP: rs863224970
rs863224970
1 1.000 0.080 1 11997316 missense variant A/G snv 0.700 1.000 8 2005 2016