Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs1370423184 1.000 0.080 7 140778018 missense variant G/C snv 4.0E-06 1
rs180177032 1.000 0.080 7 140781623 missense variant C/A snv 1
rs180177033 1.000 0.080 7 140781620 missense variant A/C snv 1