Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs17860508 0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 11
rs34383331 0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18 3
rs776022790 0.925 0.040 5 39202836 missense variant T/C snv 4.0E-06 7.0E-06 2