Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs11553699 12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs13412535 2 224010157 intron variant G/A snv 0.17 5
rs4499344 19 32582525 intron variant G/A snv 0.46 3
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 2