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: rs17535749
rs17535749
1 3 9986040 intron variant G/A snv 7.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs11761528
rs11761528
4 1.000 0.120 7 99521178 intron variant C/T snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs3901286
rs3901286
1 7 99510104 intron variant C/A snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs6707827
rs6707827
1 2 99506568 intergenic variant A/G snv 0.79 0.700 1.000 1 2019 2019
dbSNP: rs12551906
rs12551906
1 9 99356808 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 2 2017 2019
dbSNP: rs10760678
rs10760678
1 9 99317659 intergenic variant G/A snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs923724
rs923724
1 12 99246152 intron variant G/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs4082793
rs4082793
1 14 99233743 intron variant C/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs2693686
rs2693686
1 14 99206460 intron variant C/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs2372716
rs2372716
1 12 99179648 intron variant C/T snv 0.84 0.700 1.000 1 2018 2018
dbSNP: rs651548
rs651548
1 12 99166405 intron variant A/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs660879
rs660879
1 12 99160037 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs34303684
rs34303684
1 15 98976030 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs325220
rs325220
1 5 98968860 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs2715423
rs2715423
1 15 98968644 missense variant G/A snv 0.23 0.21 0.700 1.000 1 2019 2019
dbSNP: rs150992
rs150992
1 5 98939493 intron variant A/G snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs17150703
rs17150703
2 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs12227147
rs12227147
2 12 98849243 intron variant T/A snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs580809
rs580809
1 9 98756160 intron variant C/T snv 0.78 0.700 1.000 1 2017 2017
dbSNP: rs58139454
rs58139454
1 15 98686933 intron variant G/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs56803094
rs56803094
1 15 98679280 intron variant A/G snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs7334078
rs7334078
2 13 98468230 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs17574378
rs17574378
1 13 98464130 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1983864
rs1983864
1 10 98257696 missense variant T/G snv 0.39 0.29 0.700 1.000 1 2018 2018