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: rs10993994
rs10993994
15 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 0.800 1.000 3 2010 2017
dbSNP: rs2735839
rs2735839
7 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 0.800 1.000 3 2010 2018
dbSNP: rs1058205
rs1058205
3 0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 0.800 1.000 2 2010 2014
dbSNP: rs11067228
rs11067228
3 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 0.800 1.000 2 2010 2017
dbSNP: rs17632542
rs17632542
5 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 0.800 1.000 2 2010 2017
dbSNP: rs266849
rs266849
4 0.925 0.080 19 50845834 intron variant G/A snv 0.82 0.800 1.000 2 2010 2017
dbSNP: rs10788160
rs10788160
2 10 121274035 intergenic variant G/A snv 0.19 0.800 1.000 1 2010 2010
dbSNP: rs12409639
rs12409639
1 1 205669094 intron variant G/A snv 8.8E-02 0.800 1.000 1 2013 2013
dbSNP: rs1354774
rs1354774
3 0.925 0.080 19 50889862 intron variant A/G snv 0.50 0.800 1.000 1 2013 2013
dbSNP: rs16856139
rs16856139
2 1.000 0.040 1 205669336 intron variant C/G;T snv 0.800 1.000 1 2014 2014
dbSNP: rs3213764
rs3213764
3 0.925 0.080 12 14434367 missense variant A/G snv 0.47 0.42 0.800 1.000 1 2013 2013
dbSNP: rs401681
rs401681
42 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 1 2010 2010
dbSNP: rs4430796
rs4430796
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 1 2010 2010
dbSNP: rs11084596
rs11084596
3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 2 2017 2018
dbSNP: rs10023685
rs10023685
1 4 156613097 intergenic variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10486567
rs10486567
9 0.851 0.120 7 27936944 intron variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs10505477
rs10505477
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs10734875
rs10734875
1 12 14389607 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10749415
rs10749415
1 10 121425789 intergenic variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10772782
rs10772782
1 12 14439909 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10855058
rs10855058
1 X 55910389 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs10886902
rs10886902
1 10 121289750 regulatory region variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11055956
rs11055956
1 12 14381492 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11055980
rs11055980
3 1.000 0.040 12 14458588 intron variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs11199879
rs11199879
3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018