Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141173114 1.000 0.080 6 10186099 intron variant G/A;T snv 1
rs11759950 1.000 0.080 6 10226000 downstream gene variant C/T snv 0.15 1
rs427754 1.000 0.080 18 10361780 intron variant T/A;C snv 1
rs206447 1.000 0.080 18 10439989 intergenic variant A/G snv 0.33 1
rs12509636 1.000 0.080 4 105089276 intron variant C/T snv 0.39 1
rs142020459 1.000 0.080 1 10512026 intron variant C/G snv 1.8E-02 1
rs9398035 1.000 0.080 6 105593507 downstream gene variant A/C snv 0.42 1
rs4946689 1.000 0.080 6 105753733 intron variant G/A snv 0.88 1
rs12214131 0.807 0.080 6 105760046 intron variant G/A snv 0.29 7
rs17035390 1.000 0.080 1 10593565 intron variant T/C snv 3.6E-02 1
rs2242288 1.000 0.080 1 10624041 intron variant C/A snv 4.6E-02 1
rs147170006 1.000 0.080 4 106590269 intron variant T/- delins 0.14 1
rs73837363 1.000 0.080 4 106622437 intron variant G/A snv 1
rs10516537 1.000 0.080 4 106706914 intron variant A/C snv 0.84 1
rs73667301 1.000 0.080 9 106865770 intron variant A/G snv 7.6E-02 1
rs59304342 1.000 0.080 1 10693037 intron variant T/A snv 5.0E-02 1
rs4109346 1.000 0.080 4 106967631 intron variant T/A snv 0.15 1
rs76067940 1.000 0.080 4 107131838 intron variant C/T snv 2.5E-02 1
rs9846246
BBX
1.000 0.080 3 107705243 intron variant G/A;T snv 1
rs76729432 1.000 0.080 8 107793457 intergenic variant T/C snv 5.7E-02 1
rs145562694 1.000 0.080 8 107806268 intergenic variant C/A;T snv 1
rs147906392 1.000 0.080 8 107894243 intron variant C/G;T snv 1
rs2047198 1.000 0.080 8 107950399 intron variant C/G;T snv 1
rs34657911 1.000 0.080 8 108081515 intron variant G/A snv 0.17 1
rs117769774 1.000 0.080 8 108090690 intergenic variant G/A snv 2.5E-02 1