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: rs10067777
rs10067777
1 1.000 0.120 5 110490595 intron variant A/G snv 7.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs10199605
rs10199605
1 1.000 0.120 2 8354967 intron variant G/A snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs10214237
rs10214237
1 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs102275
rs102275
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.010 1.000 1 2015 2015
dbSNP: rs10249788
rs10249788
6 0.827 0.160 7 17298523 intron variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10445308
rs10445308
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs1057518775
rs1057518775
4 0.851 0.160 11 17387907 missense variant G/A;C snv 0.700 0
dbSNP: rs1058808
rs1058808
27 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 < 0.001 1 2018 2018
dbSNP: rs10738626
rs10738626
1 1.000 0.120 9 22373458 intergenic variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10791824
rs10791824
3 0.882 0.160 11 65791795 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10888499
rs10888499
1 1.000 0.120 1 152560266 intergenic variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10995251
rs10995251
1 1.000 0.120 10 62638706 intron variant C/T snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs11079788
rs11079788
2 0.925 0.120 17 47743357 intron variant C/T snv 0.23 0.010 1.000 1 2012 2012
dbSNP: rs11150780
rs11150780
2 0.925 0.120 17 81290360 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs11167761
rs11167761
2 0.925 0.120 5 141858778 intron variant G/A snv 0.14 0.010 1.000 1 2014 2014
dbSNP: rs11204971
rs11204971
2 0.925 0.120 1 152286602 intron variant A/G snv 0.15 0.710 1.000 2 2011 2012
dbSNP: rs11205006
rs11205006
1 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 0.700 1.000 1 2015 2015
dbSNP: rs112111458
rs112111458
2 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 0.710 1.000 2 2015 2017
dbSNP: rs113136594
rs113136594
2 0.925 0.120 1 152313436 missense variant G/A;C;T snv 6.0E-04; 4.0E-06; 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs11362
rs11362
13 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 0.010 1.000 1 2010 2010
dbSNP: rs11558538
rs11558538
19 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs115746363
rs115746363
3 0.882 0.120 1 152312410 stop gained G/A;C snv 6.0E-04 0.010 1.000 1 2018 2018
dbSNP: rs11584340
rs11584340
5 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 0.040 1.000 4 2011 2015
dbSNP: rs12081541
rs12081541
2 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs12130219
rs12130219
2 0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 0.700 1.000 1 2015 2015