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: rs78378222
rs78378222
37 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 0.700 1.000 5 2011 2019
dbSNP: rs11170164
rs11170164
6 0.827 0.120 12 52519884 missense variant C/T snv 5.7E-02 5.3E-02 0.700 1.000 3 2015 2019
dbSNP: rs1805007
rs1805007
25 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 0.700 1.000 3 2011 2019
dbSNP: rs401681
rs401681
42 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 3 2009 2015
dbSNP: rs7538876
rs7538876
6 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 3 2008 2015
dbSNP: rs801114
rs801114
5 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 0.700 1.000 3 2008 2015
dbSNP: rs10810657
rs10810657
7 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 2 2016 2019
dbSNP: rs1126809
rs1126809
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.700 1.000 2 2016 2019
dbSNP: rs12203592
rs12203592
38 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2019
dbSNP: rs12210050
rs12210050
8 0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 0.700 1.000 2 2011 2016
dbSNP: rs12916300
rs12916300
13 0.742 0.080 15 28165345 intron variant C/T snv 0.50 0.700 1.000 2 2016 2019
dbSNP: rs157935
rs157935
4 0.851 0.040 7 130900794 intron variant T/G snv 0.28 0.700 1.000 2 2014 2015
dbSNP: rs214782
rs214782
4 0.851 0.040 20 2301324 intron variant G/A snv 0.73 0.700 1.000 2 2014 2015
dbSNP: rs2151280
rs2151280
16 0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 0.700 1.000 2 2014 2015
dbSNP: rs2776353
rs2776353
3 0.882 0.040 21 41668857 regulatory region variant A/T snv 0.39 0.700 1.000 2 2016 2019
dbSNP: rs421284
rs421284
3 0.882 0.040 5 1325475 non coding transcript exon variant T/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs4710154
rs4710154
3 0.882 0.040 6 166981146 intron variant A/T snv 0.42 0.700 1.000 2 2016 2019
dbSNP: rs6059655
rs6059655
10 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 2 2016 2019
dbSNP: rs7006527
rs7006527
4 0.851 0.040 8 100012277 intron variant A/C;T snv 0.700 1.000 2 2014 2015
dbSNP: rs73183643
rs73183643
3 0.882 0.040 7 101775373 intergenic variant G/A snv 0.17 0.700 1.000 2 2016 2019
dbSNP: rs73635312
rs73635312
3 0.882 0.040 10 8894035 upstream gene variant G/A snv 0.20 0.700 1.000 2 2015 2016
dbSNP: rs7874604
rs7874604
3 0.882 0.040 9 22054691 intron variant T/C snv 0.58 0.700 1.000 2 2016 2019
dbSNP: rs10093547
rs10093547
3 0.882 0.040 8 76562310 intron variant T/G snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs10102591
rs10102591
3 0.882 0.040 8 80479448 intron variant G/T snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs10228836
rs10228836
3 0.882 0.040 7 50136567 intron variant A/G snv 0.49 0.700 1.000 1 2019 2019