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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12