Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555206402 0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins 26
rs1007859875 1.000 0.160 11 119092137 missense variant G/A snv 4.0E-06 1.4E-05 1
rs1057521126 1.000 0.160 11 119092785 missense variant G/A snv 1
rs1165046276 1.000 0.160 11 119089992 missense variant G/A snv 4.0E-06 1.4E-05 1
rs118204094 1.000 0.160 11 119089991 missense variant C/T snv 4.0E-06 7.0E-06 1
rs118204095 1.000 0.160 11 119091414 missense variant G/A;T snv 4.5E-05 1
rs118204096 1.000 0.160 11 119091432 missense variant G/A snv 1
rs118204097 1.000 0.160 11 119090230 stop gained C/T snv 1
rs118204098 1.000 0.160 11 119090213 missense variant G/A snv 1
rs118204099 1.000 0.160 11 119092486 missense variant T/G snv 1
rs118204100 1.000 0.160 11 119091507 stop gained G/A snv 1
rs118204101 1.000 0.160 11 119091413 missense variant C/T snv 3.8E-05 1
rs118204103 1.000 0.160 11 119088298 missense variant G/A snv 1
rs118204104 1.000 0.160 11 119088638 missense variant G/A snv 7.0E-06 1
rs118204105 1.000 0.160 11 119088647 missense variant C/A snv 1
rs118204106 1.000 0.160 11 119089084 missense variant G/T snv 7.0E-06 1
rs118204107 1.000 0.160 11 119089747 missense variant G/A snv 1
rs118204108 1.000 0.160 11 119091444 missense variant T/G snv 1
rs118204109 1.000 0.160 11 119091515 missense variant C/T snv 2.6E-05 3.5E-05 1
rs118204110 1.000 0.160 11 119092419 stop gained G/A snv 1
rs118204111 1.000 0.160 11 119092491 missense variant T/C snv 1
rs118204112 1.000 0.160 11 119092500 missense variant G/A snv 1
rs118204113 1.000 0.160 11 119092506 missense variant G/A snv 8.0E-06 1.4E-05 1
rs118204114 1.000 0.160 11 119092507 missense variant C/T snv 4.0E-06 1
rs118204115 1.000 0.160 11 119092518 missense variant C/A;G snv 1