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: rs121913105
rs121913105
30 0.653 0.600 4 1806163 missense variant A/C;T snv 0.020 1.000 2 2015 2016
dbSNP: rs121913482
rs121913482
45 0.630 0.680 4 1801837 missense variant C/T snv 0.710 1.000 1 2003 2003
dbSNP: rs28933068
rs28933068
30 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 0.010 1.000 1 2000 2000
dbSNP: rs369634007
rs369634007
10 0.882 0.080 2 112098688 missense variant A/G snv 1.6E-05 2.1E-05 0.700 1.000 1 2016 2016
dbSNP: rs587777512
rs587777512
7 0.827 0.320 4 150583180 missense variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs74315304
rs74315304
3 0.925 0.120 1 150799228 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs774568856
rs774568856
4 0.882 0.200 6 83174481 missense variant A/G snv 1.7E-05 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs78311289
rs78311289
25 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs886044555
rs886044555
3 0.925 0.080 12 47985772 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs1014959895
rs1014959895
16 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs1057518967
rs1057518967
2 1.000 0.040 7 94423102 missense variant G/A snv 0.700 0
dbSNP: rs116571438
rs116571438
2 0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 0.700 0
dbSNP: rs1209546147
rs1209546147
1 1.000 0.040 12 47980597 missense variant C/T snv 0.700 0
dbSNP: rs121912632
rs121912632
3 0.882 0.080 12 109792407 missense variant C/T snv 0.700 0
dbSNP: rs121912633
rs121912633
10 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs121912634
rs121912634
2 0.925 0.080 12 109798768 missense variant T/C snv 0.700 0
dbSNP: rs121912635
rs121912635
2 0.925 0.080 12 109788462 missense variant C/A snv 0.700 0
dbSNP: rs121912636
rs121912636
2 0.925 0.120 12 109798775 missense variant T/A;C snv 4.0E-06 0.700 0
dbSNP: rs121912637
rs121912637
5 0.851 0.160 12 109784378 missense variant G/A;C snv 0.700 0
dbSNP: rs121918130
rs121918130
18 0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 0.700 0
dbSNP: rs1251713297
rs1251713297
15 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 0.700 0
dbSNP: rs1400419650
rs1400419650
38 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs1555386022
rs1555386022
38 0.708 0.320 14 92003418 splice donor variant C/A snv 0.700 0
dbSNP: rs181011657
rs181011657
3 0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 0.700 0
dbSNP: rs267607147
rs267607147
2 0.925 0.120 12 109784379 missense variant G/A;C snv 0.700 0