Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs939317 3 184328011 intron variant A/C;G snv 0.76 0.80 1
rs3914188 3 184292260 3 prime UTR variant G/C snv 0.73 0.73 2
rs1131017 0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs1933437 13 28050157 missense variant G/A snv 0.60 0.53 2
rs999885 0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 1
rs365132 5 176951573 synonymous variant G/T snv 0.51 0.58 2
rs2725405 17 81246424 missense variant G/C snv 0.49 0.36 1
rs2297605 9 124493169 intron variant G/A;C;T snv 0.49; 3.7E-05; 8.2E-06 1
rs9652589 16 20359494 missense variant C/T snv 0.44 0.46 2
rs913588 9 7174673 missense variant G/A snv 0.42 0.43 1
rs707938 6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs2836950 21 39232503 splice region variant C/A;G snv 9.0E-06; 0.37 1
rs1799949 17 43093449 synonymous variant G/A snv 0.35 0.31 2
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 5
rs66461782 1 71067604 intron variant A/T snv 0.32 0.27 2
rs4889 0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 1
rs3133974 8 93734470 synonymous variant G/A;C;T snv 2.6E-04; 4.0E-06; 9.2E-05; 0.28 1
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs34811474 1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs3746619 0.925 0.200 20 56248749 5 prime UTR variant C/A snv 0.14 0.21 1
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs17854357 11 65834089 splice region variant G/C;T snv 0.12; 5.8E-05 1
rs61744130 19 53576813 missense variant T/C snv 5.9E-02 3.9E-02 1
rs80170948 5 64724489 missense variant T/G snv 3.0E-02 2.8E-02 2
rs72661148 18 47845324 synonymous variant A/G snv 2.2E-02 2.4E-02 1