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: rs58415480
rs58415480
2 1.000 6 152241136 intron variant C/G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs78378222
rs78378222
37 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 0.700 1.000 3 2018 2019
dbSNP: rs10917151
rs10917151
3 0.925 0.040 1 22096228 3 prime UTR variant G/A snv 0.14 0.700 1.000 2 2018 2019
dbSNP: rs117245733
rs117245733
2 1.000 13 40149807 intron variant G/A snv 1.3E-02 0.700 1.000 2 2018 2019
dbSNP: rs149934734
rs149934734
2 1.000 11 108444879 intron variant C/T snv 1.6E-02 0.700 1.000 2 2018 2019
dbSNP: rs16991615
rs16991615
6 0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 0.700 1.000 2 2018 2019
dbSNP: rs7907606
rs7907606
8 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 2 2018 2019
dbSNP: rs7986407
rs7986407
4 0.882 0.120 13 40605661 intron variant A/G snv 0.38 0.700 1.000 2 2018 2019
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs10508765
rs10508765
2 1.000 10 31679855 intergenic variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10815466
rs10815466
2 1.000 9 680714 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs10835889
rs10835889
2 1.000 11 32348834 intergenic variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10929757
rs10929757
2 1.000 2 11562535 missense variant A/C snv 0.54 0.44 0.700 1.000 1 2018 2018
dbSNP: rs10976689
rs10976689
2 1.000 9 804886 intergenic variant A/G snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs11031006
rs11031006
8 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs11031731
rs11031731
3 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11178393
rs11178393
2 1.000 12 70756878 intron variant T/C snv 8.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs11246001
rs11246001
2 1.000 11 210899 non coding transcript exon variant C/T snv 4.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs11246003
rs11246003
2 1.000 11 213723 non coding transcript exon variant T/G snv 4.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs116251328
rs116251328
2 1.000 6 34209733 intergenic variant T/A snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs11987640
rs11987640
2 1.000 8 4584258 intron variant G/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12037376
rs12037376
3 0.925 0.040 1 22135618 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs12224688
rs12224688
2 1.000 11 32305471 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs12392108
rs12392108
2 1.000 X 132180234 intergenic variant T/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs12484776
rs12484776
2 1.000 22 40256869 intron variant A/G snv 0.19 0.700 1.000 1 2011 2011