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: rs121918461
rs121918461
12 0.827 0.240 12 112450362 missense variant A/C;G;T snv 0.720 1.000 27 2001 2018
dbSNP: rs121918462
rs121918462
13 0.742 0.320 12 112450398 missense variant C/T snv 0.740 1.000 24 2002 2015
dbSNP: rs397517154
rs397517154
16 0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 19 2007 2018
dbSNP: rs121918453
rs121918453
19 0.732 0.280 12 112450394 missense variant G/A;C;T snv 0.710 1.000 18 2002 2009
dbSNP: rs397507505
rs397507505
5 0.827 0.240 12 112450352 missense variant A/C;G;T snv 0.710 1.000 17 2003 2015
dbSNP: rs397507520
rs397507520
39 0.658 0.520 12 112453279 missense variant G/C;T snv 0.710 1.000 17 2002 2013
dbSNP: rs121918456
rs121918456
13 0.752 0.280 12 112473023 missense variant A/C;G snv 0.710 1.000 15 2002 2011
dbSNP: rs28933386
rs28933386
15 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 0.720 1.000 15 2001 2019
dbSNP: rs397507509
rs397507509
9 0.807 0.240 12 112450359 missense variant G/C;T snv 0.710 1.000 14 2002 2014
dbSNP: rs121918459
rs121918459
47 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 0.720 0.923 13 2001 2013
dbSNP: rs397507540
rs397507540
8 0.851 0.160 12 112489048 missense variant C/A;T snv 0.700 1.000 13 2004 2014
dbSNP: rs121918458
rs121918458
8 0.807 0.320 12 112489080 missense variant T/A;G snv 0.700 1.000 12 2002 2013
dbSNP: rs397507545
rs397507545
20 0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 0.710 1.000 12 2003 2019
dbSNP: rs121918466
rs121918466
14 0.752 0.280 12 112450416 missense variant A/G snv 0.730 1.000 11 2001 2009
dbSNP: rs397507549
rs397507549
13 0.742 0.240 12 112489104 missense variant C/A;G snv 0.700 1.000 10 2005 2012
dbSNP: rs80338796
rs80338796
37 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 0.700 1.000 10 1992 2018
dbSNP: rs104894365
rs104894365
9 0.827 0.320 12 25245345 missense variant C/T snv 0.720 1.000 9 2006 2018
dbSNP: rs121918455
rs121918455
31 0.695 0.440 12 112477720 missense variant A/C;G snv 0.710 1.000 9 2002 2017
dbSNP: rs267607048
rs267607048
16 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 0.750 1.000 9 2009 2019
dbSNP: rs397507501
rs397507501
5 0.882 0.160 12 112446385 missense variant A/G snv 0.710 1.000 9 2002 2013
dbSNP: rs397507514
rs397507514
10 0.790 0.240 12 112450408 missense variant G/C;T snv 0.710 1.000 9 2001 2011
dbSNP: rs397507517
rs397507517
8 0.827 0.160 12 112450497 missense variant A/C snv 0.700 1.000 9 2002 2011
dbSNP: rs397507529
rs397507529
5 0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 0.700 1.000 9 2001 2011
dbSNP: rs104894364
rs104894364
2 0.925 0.160 12 25227351 missense variant G/A snv 0.710 1.000 8 2006 2013
dbSNP: rs121918454
rs121918454
17 0.742 0.280 12 112450395 missense variant C/A;G;T snv 0.710 1.000 8 2001 2014