Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18