Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25