Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2820443 | 0.882 | 0.120 | 1 | 219580167 | regulatory region variant | T/C | snv | 0.23 | 8 | ||
rs13241427 | 1.000 | 7 | 1249003 | regulatory region variant | G/T | snv | 0.72 | 6 | |||
rs2145270 | 20 | 6641038 | regulatory region variant | C/T | snv | 0.61 | 4 | ||||
rs41310284 | 10 | 100687890 | intergenic variant | C/A;T | snv | 3 | |||||
rs994014 | 4 | 81244636 | intergenic variant | T/C | snv | 0.43 | 3 | ||||
rs2635727 | 1.000 | 0.080 | 6 | 50853227 | downstream gene variant | T/C;G | snv | 2 | |||
rs4694504 | 4 | 72630974 | intergenic variant | A/G;T | snv | 2 | |||||
rs6492538 | 13 | 91341492 | intergenic variant | A/C | snv | 0.83 | 2 | ||||
rs7306275 | 12 | 49856328 | upstream gene variant | G/A | snv | 0.29 | 2 | ||||
rs112416074 | 7 | 148950668 | intergenic variant | -/G | delins | 0.14 | 1 | ||||
rs11614785 | 12 | 50486639 | intergenic variant | C/G | snv | 0.24 | 1 | ||||
rs12971970 | 19 | 47056015 | intergenic variant | T/A;C | snv | 1 | |||||
rs13011472 | 2 | 57734467 | intergenic variant | C/G | snv | 0.40 | 1 | ||||
rs1317415 | 5 | 158525396 | intron variant | T/A;C | snv | 1 | |||||
rs17781552 | 1 | 203550520 | intergenic variant | G/A | snv | 0.58 | 1 | ||||
rs2607733 | 3 | 14103134 | intergenic variant | T/A;C | snv | 1 | |||||
rs356429 | 5 | 139693558 | intron variant | C/T | snv | 0.30 | 1 | ||||
rs56372408 | 2 | 171560293 | downstream gene variant | A/G | snv | 0.17 | 1 | ||||
rs5779197 | 1 | 184040693 | upstream gene variant | A/-;AA;AAA;AAAA;AAAAA | delins | 1 | |||||
rs62107261 | 2 | 422144 | non coding transcript exon variant | T/C | snv | 2.9E-02 | 1 | ||||
rs6731872 | 2 | 624205 | intergenic variant | T/G | snv | 0.85 | 1 | ||||
rs7039458 | 9 | 84025084 | intergenic variant | G/A | snv | 0.70 | 1 | ||||
rs71336392 | 18 | 60183695 | intergenic variant | TCT/- | delins | 0.24 | 1 | ||||
rs9469762 | 6 | 34268653 | intron variant | G/A;T | snv | 1 | |||||
rs3817428 | 15 | 88872016 | missense variant | C/G | snv | 0.20 | 0.20 | 3 |