Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10123382 9 4757649 intron variant G/A snv 0.28 1
rs10277403 7 47594213 intergenic variant T/A;C snv 1
rs10463065 5 177322927 intergenic variant C/A;G snv 1
rs10495161 1 220963330 regulatory region variant C/T snv 0.14 1
rs10750385 11 128067871 regulatory region variant A/C;G snv 0.76 1
rs10762861 10 79377440 upstream gene variant A/G snv 0.80 1
rs11039624 11 48269014 downstream gene variant G/A snv 2.6E-02 1
rs11130543 3 56702914 regulatory region variant G/T snv 0.37 1
rs111639853 17 47983593 intron variant C/T snv 2.1E-02 1
rs11170516 12 53358908 intergenic variant G/A snv 0.16 1
rs111977000 11 126147164 TF binding site variant C/T snv 0.41 1
rs11230876 11 62028924 intergenic variant G/C;T snv 1
rs112471280 3 47489105 intergenic variant G/A snv 4.5E-02 1
rs112984321 20 36979076 intergenic variant A/G snv 0.16 1
rs113549824 4 105030032 intron variant C/A snv 3.6E-02 1
rs113938611 20 33701916 downstream gene variant G/A snv 6.7E-02 1
rs114748586 4 122058283 intergenic variant G/A;T snv 1
rs115299044 6 34268685 intron variant C/G snv 2.8E-02 1
rs116036161 3 142253182 intergenic variant T/A snv 1.3E-02 1
rs11695646 2 231720097 intergenic variant A/G snv 0.26 1
rs117106225 16 30448962 upstream gene variant C/A snv 3.2E-02 1
rs117265206 14 64688197 regulatory region variant A/T snv 1.7E-02 1
rs117543466 16 557131 upstream gene variant C/T snv 2.9E-02 1
rs117976152 6 135841284 intergenic variant G/A snv 1.1E-02 1
rs11807602 1 93073392 intergenic variant C/G snv 0.32 1