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: rs10098598
rs10098598
1 1.000 0.040 8 116848536 intron variant C/T snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs10954695
rs10954695
1 1.000 0.040 7 82927912 intron variant G/A snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs11849937
rs11849937
1 1.000 0.040 14 78645876 intron variant C/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs11906570
rs11906570
1 1.000 0.040 20 64131898 intron variant C/A snv 0.700 1.000 1 2019 2019
dbSNP: rs12405527
rs12405527
1 1.000 0.040 1 101217609 regulatory region variant G/A snv 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs140724264
rs140724264
1 1.000 0.040 9 95602990 intron variant A/G snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1990042
rs1990042
1 1.000 0.040 7 44936750 intergenic variant T/A;C snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs3851101
rs3851101
1 1.000 0.040 11 123653388 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs62198555
rs62198555
1 1.000 0.040 2 185171397 intergenic variant G/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs703610
rs703610
1 1.000 0.040 12 103617146 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019