Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1968252 | 19 | 7782850 | upstream gene variant | G/A;T | snv | 5 | |||||
rs201950044 | 1 | 161639782 | intergenic variant | G/T | snv | 5 | |||||
rs2208568 | 1 | 235926855 | intergenic variant | T/A;C;G | snv | 5 | |||||
rs34061361 | 13 | 28044450 | intron variant | AAA/-;A;AA;AAAA | delins | 5 | |||||
rs3917914 | 1 | 36482287 | intron variant | G/A;T | snv | 5 | |||||
rs397731840 | 8 | 129599504 | intron variant | TT/-;T;TTT;TTTT;TTTTT | delins | 5 | |||||
rs397933924 | 10 | 97314229 | upstream gene variant | -/CAGGTTCAAGCGA | ins | 5 | |||||
rs6500550 | 16 | 3696240 | intron variant | C/G;T | snv | 5 | |||||
rs66505542 | 11 | 116752498 | intron variant | AA/-;A;AAA | delins | 5 | |||||
rs73316435 | 0.882 | 17 | 47252111 | upstream gene variant | C/A;T | snv | 5 | ||||
rs8179 | 0.882 | 0.080 | 7 | 92606850 | 3 prime UTR variant | T/A;C;G | snv | 5 | |||
rs8705 | 11 | 128459018 | 3 prime UTR variant | G/A;T | snv | 5 | |||||
rs9979383 | 0.925 | 0.200 | 21 | 35343463 | intron variant | C/G;T | snv | 5 | |||
rs10206089 | 2 | 61476184 | intron variant | G/A | snv | 4 | |||||
rs10795656 | 1.000 | 0.080 | 10 | 8553876 | intergenic variant | G/A;T | snv | 4 | |||
rs11204682 | 1 | 150623061 | intron variant | G/A;T | snv | 4 | |||||
rs11405616 | 5 | 142130697 | intron variant | A/-;AA;AAA;AAAA | delins | 4 | |||||
rs11428934 | 19 | 48640988 | intron variant | -/G | ins | 4 | |||||
rs11734460 | 4 | 711285 | intron variant | C/A;T | snv | 4 | |||||
rs13138355 | 4 | 82624823 | upstream gene variant | C/A;T | snv | 4 | |||||
rs14408 | 11 | 308314 | missense variant | T/C;G | snv | 0.53 | 4 | ||||
rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 | |||
rs2239630 | 0.925 | 0.160 | 14 | 23120140 | upstream gene variant | A/C;G | snv | 4 | |||
rs301807 | 0.925 | 0.080 | 1 | 8424763 | intron variant | A/G;T | snv | 4 | |||
rs34293785 | 1 | 65671509 | intergenic variant | T/C | snv | 4 |