Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs12938031 0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs7867155 0.925 0.080 9 96065532 intron variant C/T snv 0.13 2
rs9980603 0.925 0.080 21 40514656 intron variant T/C snv 0.40 2