Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs934945 0.827 0.200 2 238246412 missense variant C/T snv 0.21 0.15 10
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23