Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs778293 | 0.807 | 0.120 | 13 | 105516850 | intergenic variant | C/A;T | snv | 7 | |||
rs1409851868 | 0.882 | 0.080 | 3 | 89399325 | missense variant | A/G | snv | 6 | |||
rs35753505 | 0.827 | 0.080 | 8 | 31616625 | intergenic variant | T/A;C | snv | 6 | |||
rs3749034 | 0.827 | 0.040 | 2 | 170816965 | 5 prime UTR variant | G/A;T | snv | 6 | |||
rs3803300 | 0.827 | 0.120 | 14 | 104803442 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs3817190 | 0.851 | 0.080 | 12 | 121274274 | missense variant | T/A;G | snv | 0.38 | 6 | ||
rs4500567 | 0.807 | 0.200 | 12 | 71166082 | intron variant | G/A;C | snv | 6 | |||
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 6 | |||
rs707284 | 0.807 | 0.080 | 2 | 211974321 | intron variant | T/A;C | snv | 6 | |||
rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 5 | |||
rs1106854 | 0.827 | 0.080 | 2 | 75050887 | intron variant | T/C;G | snv | 5 | |||
rs11789399 | 0.882 | 0.040 | 9 | 118597008 | intergenic variant | G/A;C | snv | 5 | |||
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs2721800 | 0.851 | 0.040 | 7 | 24652933 | intron variant | G/A;C;T | snv | 5 | |||
rs28456 | 0.925 | 0.120 | 11 | 61822009 | intron variant | A/C;G | snv | 5 | |||
rs3831455 | 0.827 | 0.080 | 11 | 113904828 | 5 prime UTR variant | GAG/- | delins | 5 | |||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs9951150 | 0.851 | 0.040 | 18 | 55153893 | intergenic variant | A/G;T | snv | 5 | |||
rs10835210 | 0.882 | 0.040 | 11 | 27674363 | intron variant | C/A;G | snv | 4 | |||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs12649507 | 0.851 | 0.080 | 4 | 55514317 | intron variant | G/A;T | snv | 4 | |||
rs141252918 | 0.882 | 0.040 | 6 | 151506923 | intron variant | G/A;C | snv | 4 | |||
rs17154917 | 0.851 | 0.040 | 7 | 81207393 | intergenic variant | G/A;T | snv | 4 | |||
rs17211233 | 0.882 | 0.040 | 5 | 81072944 | intron variant | T/A;C | snv | 4 |