Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4251552 1.000 0.040 12 43787338 3 prime UTR variant A/G snv 4.7E-02 1
rs1365483160 1.000 0.040 9 128836915 missense variant G/A snv 1
rs2067085 1.000 0.040 16 50699948 synonymous variant C/A;G snv 4.1E-06; 0.33 1
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5
rs2285932 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs2072136 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs121918338 0.807 0.160 9 136370362 stop gained G/A snv 1.2E-05 7.0E-06 7
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs5743704 0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs1556620697 0.827 0.360 X 124365758 splice region variant C/G snv 10
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147