Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3918149 1.000 0.040 6 32968596 5 prime UTR variant G/A snv 0.11 1
rs183899632 1.000 0.040 8 67746023 missense variant C/A;T snv 5.6E-05; 4.0E-05 1
rs137852777 1.000 0.040 6 52452742 missense variant G/A snv 4.8E-05 1
rs137852778 1.000 0.040 6 52454128 missense variant G/A;T snv 2.0E-05 1
rs142458862 1.000 0.040 6 52492274 missense variant T/G snv 1.8E-04 1.2E-04 1
rs149998588 1.000 0.040 6 52479759 stop gained C/T snv 3.2E-05 1.4E-05 1
rs17851770 1.000 0.040 6 52492273 missense variant A/C snv 6.2E-02 6.2E-02 1
rs200191497 1.000 0.040 6 52438562 missense variant C/T snv 7.2E-05 1.4E-05 1
rs371151471 1.000 0.040 6 52465092 missense variant C/T snv 1.2E-03 2.0E-04 1
rs377286138 1.000 0.040 6 52479064 missense variant C/T snv 1.1E-04 7.0E-05 1
rs3804505 1.000 0.040 6 52438563 missense variant G/A;T snv 6.0E-02 1
rs527295360 1.000 0.040 6 52465035 missense variant C/T snv 2.1E-04 1.5E-04 1
rs527539103 1.000 0.040 6 52479703 missense variant A/G snv 1
rs534797617 1.000 0.040 6 52479212 missense variant A/C;G snv 1.6E-05 1
rs543160745 1.000 0.040 6 52424148 missense variant A/G snv 4.0E-06; 7.6E-05 1
rs574948354 1.000 0.040 6 52492310 missense variant A/G snv 8.0E-05 1
rs745600475 1.000 0.040 6 52438476 missense variant G/A;T snv 1.2E-05; 4.0E-06 1
rs764096785 1.000 0.040 6 52438370 missense variant C/T snv 1.2E-05 3.5E-05 1
rs767833659 1.000 0.040 6 52465042 missense variant A/G snv 4.0E-06 1
rs772265107 1.000 0.040 6 52490165 missense variant G/A;T snv 4.8E-05; 4.0E-06 1
rs779322943 1.000 0.040 6 52479211 missense variant T/C snv 4.0E-06 1
rs780571007 1.000 0.040 6 52454113 missense variant A/G snv 3.2E-05 5.6E-05 1
rs781665913 1.000 0.040 6 52452688 missense variant G/A snv 6.4E-05 8.4E-05 1
rs2208592 1.000 0.040 X 44235439 missense variant G/A;T snv 0.11 1
rs3743123 1.000 0.040 15 34752856 synonymous variant G/A snv 0.32 0.31 1