Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 19 | ||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs10821907 | 0.776 | 0.080 | 10 | 50888694 | upstream gene variant | C/T | snv | 0.20 | 12 | ||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 7 | |||
rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 7 | ||
rs9895661 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 7 | ||
rs13146355 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 6 | ||
rs1533988 | 7 | 1253374 | intergenic variant | A/T | snv | 0.59 | 6 | ||||
rs9472135 | 0.925 | 0.120 | 6 | 43842065 | intron variant | T/A;C;G | snv | 6 | |||
rs11072567 | 15 | 76006403 | intron variant | A/G | snv | 0.43 | 5 | ||||
rs128494 | 21 | 36461960 | intron variant | T/C | snv | 0.72 | 4 | ||||
rs2337106 | 18 | 48934533 | intron variant | C/A;G | snv | 4 | |||||
rs6484504 | 11 | 31403276 | intron variant | T/C | snv | 0.79 | 3 | ||||
rs7766720 | 6 | 106725104 | non coding transcript exon variant | T/C | snv | 0.16 | 3 | ||||
rs11564722 | 11 | 2157100 | intron variant | C/T | snv | 0.25 | 2 | ||||
rs4859682 | 4 | 76489165 | intron variant | C/A | snv | 0.33 | 2 | ||||
rs6880621 | 5 | 34504277 | intergenic variant | G/A | snv | 0.55 | 2 | ||||
rs7187776 | 16 | 28846324 | 5 prime UTR variant | A/C;G | snv | 2 | |||||
rs8080123 | 17 | 61165553 | intron variant | T/G | snv | 0.74 | 2 |