Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs9468925 0.851 0.040 6 31291060 intron variant G/A snv 0.44 5
rs11966200 0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 4
rs13208776 0.882 0.040 6 168540944 intron variant G/A;C snv 3
rs7758128 0.882 0.040 6 32377506 intron variant C/A;T snv 4.2E-02 3