Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17