Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 15 | ||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs2179593 | 0.790 | 0.080 | 20 | 44031646 | intron variant | C/A | snv | 0.71 | 11 | ||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs4449583 | 5 | 1284020 | intron variant | C/T | snv | 0.25 | 5 | ||||
rs55709272 | 2 | 113109711 | intron variant | T/A;C | snv | 5 | |||||
rs7955734 | 12 | 4223993 | intergenic variant | C/G | snv | 0.22 | 5 | ||||
rs9804550 | 11 | 5164863 | intergenic variant | T/A;C | snv | 5 | |||||
rs16928078 | 11 | 2298783 | intron variant | C/T | snv | 0.15 | 4 | ||||
rs11211480 | 1 | 47227548 | non coding transcript exon variant | A/G | snv | 0.42 | 3 | ||||
rs11190134 | 10 | 99522443 | upstream gene variant | G/A | snv | 0.36 | 2 | ||||
rs139974673 | 15 | 43735687 | intron variant | T/C | snv | 2.0E-02 | 2 | ||||
rs1977080 | 22 | 43934151 | intron variant | C/T | snv | 0.19 | 2 | ||||
rs7803075 | 7 | 131057307 | intron variant | A/G | snv | 0.50 | 2 |