Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs10905453 1.000 0.080 10 8702058 regulatory region variant A/G;T snv 1
rs11072508 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 1
rs11632715 1.000 0.080 15 32712046 intergenic variant G/A snv 0.47 1
rs11694911 1.000 0.080 2 10433072 regulatory region variant C/T snv 0.12 1
rs11987193 1.000 0.080 8 29478491 intergenic variant T/C snv 0.71 1
rs12759486 1.000 0.080 1 221893194 intron variant C/T snv 0.47 1
rs12902616 1.000 0.080 15 32704974 regulatory region variant A/G;T snv 1
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 1
rs158552 1.000 0.080 20 54125959 TF binding site variant C/G;T snv 1
rs16888589 1.000 0.080 8 116623363 intergenic variant A/G snv 9.5E-02 1
rs16941835 0.790 0.080 16 86662114 intron variant G/C snv 0.20 1
rs17051076 1.000 0.080 4 130729712 intergenic variant G/A;T snv 4.7E-02 1
rs17217119 1.000 0.080 20 54126051 regulatory region variant A/G snv 0.19 1
rs1944682 1.000 0.080 11 121771082 intron variant G/T snv 0.58 1
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 1
rs2423297 1.000 0.080 20 7840844 regulatory region variant G/A;C snv 0.34 1
rs27437 1.000 0.080 5 132101268 regulatory region variant A/G snv 0.40 1
rs377426 1.000 0.080 4 111841680 intron variant G/T snv 0.55 1
rs4749812 1.000 0.080 10 8695601 intergenic variant G/C snv 0.42 1
rs6038071 1.000 0.080 20 584433 regulatory region variant C/T snv 0.14 1
rs6061231 0.790 0.080 20 62381861 downstream gene variant C/A snv 0.28 1
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 1
rs66475048 1.000 0.080 11 63572600 downstream gene variant G/A snv 0.17 1
rs67052019 1.000 0.080 1 109822839 regulatory region variant TGTAGGGGCACAGAGAGA/-;TGTAGGGGCACAGAGAGATGTAGGGGCACAGAGAGA delins 1