Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 6 | ||||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
rs11076175 | 16 | 56972466 | intron variant | A/G | snv | 0.20 | 5 | ||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 5 | ||||
rs289714 | 16 | 56973539 | intron variant | G/A | snv | 0.76; 4.0E-06 | 0.70 | 5 | |||
rs11076176 | 16 | 56973534 | intron variant | T/A;G | snv | 2.4E-05; 0.22 | 4 | ||||
rs12720922 | 16 | 56966973 | intron variant | G/A | snv | 0.23 | 4 | ||||
rs1532625 | 16 | 56971389 | splice region variant | C/T | snv | 0.40 | 0.34 | 4 | |||
rs7205804 | 16 | 56970977 | intron variant | G/A | snv | 0.34 | 4 | ||||
rs12720900 | 16 | 56977385 | non coding transcript exon variant | T/C | snv | 8.9E-04 | 3 | ||||
rs289718 | 16 | 56976020 | intron variant | C/T | snv | 0.64 | 3 | ||||
rs289719 | 16 | 56976029 | intron variant | T/C | snv | 0.66 | 3 | ||||
rs11076174 | 16 | 56969234 | intron variant | T/C | snv | 0.10 | 2 | ||||
rs289742 | 16 | 56983850 | downstream gene variant | C/G | snv | 0.80 | 2 | ||||
rs9923854 | 16 | 56983090 | intron variant | T/G | snv | 0.10 | 2 | ||||
rs118146573 | 16 | 56967026 | intron variant | G/A | snv | 9.4E-02 | 1 | ||||
rs891141 | 16 | 56969811 | intron variant | G/T | snv | 0.96 | 1 | ||||
rs891142 | 16 | 56970065 | intron variant | T/C | snv | 0.97 | 1 | ||||
rs711752 | 1.000 | 0.040 | 16 | 56962299 | splice region variant | G/A;C | snv | 6 | |||
rs9939224 | 1.000 | 0.040 | 16 | 56968820 | intron variant | T/G | snv | 0.75 | 6 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 5 | ||
rs5880 | 0.827 | 0.040 | 16 | 56981179 | missense variant | G/C | snv | 5.2E-02 | 3.7E-02 | 2 | |
rs5883 | 1.000 | 0.040 | 16 | 56973441 | synonymous variant | C/T | snv | 5.1E-02 | 6.6E-02 | 2 | |
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 |