Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146890554 17 40017384 3 prime UTR variant C/T snv 9.6E-03 5
rs757308934 17 40016599 missense variant G/A snv 9.2E-05 4.9E-05 2
rs1042658 1.000 0.080 17 40017649 3 prime UTR variant C/G;T snv 1
rs25645 17 40016890 synonymous variant G/A snv 0.39 0.29 1