Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64