Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10243383 | 1.000 | 0.040 | 7 | 22242733 | intron variant | C/T | snv | 0.51 | 2 | ||
rs114969316 | 1.000 | 0.040 | 6 | 88460643 | intergenic variant | A/G | snv | 1.6E-02 | 2 | ||
rs115319209 | 1.000 | 0.040 | 14 | 75298968 | downstream gene variant | G/A | snv | 1.0E-02 | 2 | ||
rs12036147 | 1.000 | 0.040 | 1 | 239835413 | intron variant | A/G;T | snv | 2 | |||
rs141980369 | 1.000 | 0.040 | 6 | 118888344 | intron variant | G/A | snv | 6.1E-02 | 2 | ||
rs142383097 | 1.000 | 0.040 | 1 | 10461101 | 3 prime UTR variant | A/C;G | snv | 2.0E-02 | 2 | ||
rs143916815 | 1.000 | 0.040 | 15 | 39191714 | intron variant | G/C | snv | 1.0E-02 | 2 | ||
rs35426224 | 1.000 | 0.040 | 14 | 99783354 | intron variant | G/A | snv | 5.2E-02 | 2 | ||
rs59711329 | 1.000 | 0.040 | 19 | 57901128 | intron variant | G/A;C | snv | 2 | |||
rs6487668 | 1.000 | 0.040 | 12 | 9200312 | intron variant | C/A | snv | 0.78 | 2 | ||
rs734152 | 1.000 | 0.040 | 12 | 109759971 | intron variant | G/C;T | snv | 2 | |||
rs76782312 | 1.000 | 0.040 | 6 | 109643865 | intron variant | C/T | snv | 1.6E-02 | 2 | ||
rs7897478 | 1.000 | 0.040 | 10 | 29945955 | intergenic variant | A/C;G | snv | 2 | |||
rs9432230 | 1.000 | 0.040 | 1 | 230882365 | intron variant | C/T | snv | 6.4E-02 | 2 | ||
rs9487114 | 1.000 | 0.040 | 6 | 109460597 | intron variant | T/C;G | snv | 2 |