Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10058621 | 5 | 51259335 | intergenic variant | T/C | snv | 6.0E-02 | 1 | ||||
rs11074779 | 16 | 26440122 | intergenic variant | T/C | snv | 0.16 | 1 | ||||
rs12436690 | 14 | 97119552 | intron variant | G/A | snv | 0.12 | 1 | ||||
rs12990252 | 2 | 35861457 | intergenic variant | G/C | snv | 0.18 | 1 | ||||
rs13166268 | 5 | 121024223 | intergenic variant | C/G | snv | 9.2E-02 | 1 | ||||
rs140454225 | 16 | 1003856 | upstream gene variant | T/C;G | snv | 1 | |||||
rs1449587 | 13 | 48839332 | regulatory region variant | C/T | snv | 0.31 | 1 | ||||
rs145471199 | 7 | 9407441 | intergenic variant | A/G;T | snv | 1 | |||||
rs150900094 | 15 | 87284961 | intergenic variant | A/C | snv | 2.9E-02 | 1 | ||||
rs35551159 | 12 | 60075450 | intergenic variant | C/A;T | snv | 1 | |||||
rs4762194 | 12 | 97789941 | intergenic variant | G/A | snv | 0.20 | 1 | ||||
rs4776997 | 15 | 67858585 | intron variant | A/G;T | snv | 0.77 | 1 | ||||
rs6020113 | 20 | 37674643 | upstream gene variant | G/A | snv | 9.2E-02 | 1 | ||||
rs6813517 | 4 | 167601600 | intergenic variant | T/C | snv | 0.17 | 1 | ||||
rs74938950 | 20 | 12281822 | intron variant | C/T | snv | 1.2E-02 | 1 | ||||
rs7557162 | 2 | 177057129 | intron variant | A/C;T | snv | 1 | |||||
rs8073765 | 17 | 13726414 | regulatory region variant | T/C | snv | 0.26 | 1 | ||||
rs932350 | 1 | 4793628 | downstream gene variant | T/A;C | snv | 1 | |||||
rs9528384 | 13 | 61728432 | regulatory region variant | A/G | snv | 0.23 | 1 | ||||
rs5747035 | 22 | 17237716 | intron variant | T/C | snv | 0.15 | 1 | ||||
rs6830160 | 4 | 25377604 | intron variant | G/A;T | snv | 8.1E-02 | 1 | ||||
rs111882035 | 4 | 85495401 | intron variant | A/G | snv | 1.9E-02 | 1 | ||||
rs8067235 | 17 | 81050837 | intron variant | G/A | snv | 0.30 | 1 | ||||
rs78532272 | 20 | 288517 | intron variant | G/A;C | snv | 1 | |||||
rs11775026 | 8 | 73264813 | intergenic variant | T/C | snv | 5.9E-02 | 1 |