Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 30
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 24
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs587776802 1.000 0.080 3 179234358 frameshift variant -/A delins 2