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 47
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs11553699 12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs56043070 1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs139141690 7 101856650 intron variant G/A snv 2.2E-03 3
rs8073060 17 35548243 missense variant T/A snv 0.32 0.34 3
rs3748136 8 9172650 intron variant G/A snv 0.21 2