Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs937282 1.000 0.080 12 68808017 upstream gene variant C/G snv 0.56 1