Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs3765209 0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs13146355 1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs11920090 1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs12922822 1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs1264347 1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 4
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs3812035 1.000 0.040 5 177390142 3 prime UTR variant G/A;T snv 4
rs10084572 1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs1052700 1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 3
rs11124945 1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs113296370 1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs12107 1.000 0.040 22 36281936 3 prime UTR variant G/A;T snv 3
rs1228534100 1.000 0.040 12 120978892 missense variant G/A snv 7.0E-06 3
rs145590578 1.000 0.040 6 160236104 intron variant GTT/- delins 9.8E-02 3
rs1556751 1.000 0.040 9 68818296 intron variant G/A snv 0.63 3
rs1906436 1.000 0.040 15 53590245 intron variant T/C snv 0.32 3
rs192902098 1.000 0.040 13 27920235 missense variant C/A;G;T snv 2.6E-03; 3.4E-04; 5.6E-05 3
rs1974990 1.000 0.040 2 169790406 non coding transcript exon variant G/T snv 0.90 3