Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2662411 | 1.000 | 5 | 10133592 | upstream gene variant | G/A;C | snv | 5 | ||||
rs28508297 | 1.000 | 14 | 106125683 | upstream gene variant | G/C | snv | 8.8E-02 | 5 | |||
rs2516928 | 1.000 | 14 | 106587377 | upstream gene variant | C/T | snv | 7.3E-02 | 5 | |||
rs2157999 | 1.000 | 12 | 111266635 | intron variant | G/A | snv | 8.1E-02 | 5 | |||
rs7719972 | 1.000 | 5 | 117580137 | intergenic variant | G/A | snv | 8.5E-02 | 5 | |||
rs7130078 | 1.000 | 11 | 129980320 | intron variant | G/A | snv | 5.5E-02 | 5 | |||
rs7126904 | 1.000 | 11 | 130190674 | missense variant | G/A | snv | 2.2E-02 | 8.8E-02 | 5 | ||
rs78430868 | 1.000 | 11 | 131630365 | intron variant | C/A | snv | 5.7E-02 | 5 | |||
rs2801270 | 1.000 | 21 | 13297803 | intergenic variant | A/G | snv | 7.8E-02 | 5 | |||
rs2789845 | 1.000 | 9 | 133934793 | intron variant | C/T | snv | 0.80 | 5 | |||
rs28404523 | 1.000 | 17 | 13627527 | intergenic variant | G/A | snv | 0.23 | 5 | |||
rs13391004 | 1.000 | 2 | 136609937 | intergenic variant | G/A | snv | 9.1E-02 | 5 | |||
rs9285942 | 1.000 | 5 | 139413007 | 3 prime UTR variant | G/A | snv | 6.9E-02 | 5 | |||
rs2070715 | 1.000 | 5 | 142644691 | intron variant | T/C;G | snv | 5 | ||||
rs1868175 | 1.000 | 3 | 143686482 | intron variant | A/G | snv | 0.75 | 5 | |||
rs7755842 | 1.000 | 6 | 144158325 | intron variant | A/T | snv | 0.10 | 5 | |||
rs60463810 | 1.000 | 6 | 148588135 | intergenic variant | C/T | snv | 0.12 | 5 | |||
rs61733346 | 1.000 | 7 | 151202976 | missense variant | C/G | snv | 9.2E-02 | 5 | |||
rs6596833 | 1.000 | 6 | 1545111 | intergenic variant | T/C | snv | 1.0E-01 | 5 | |||
rs2800778 | 1.000 | 1 | 164652278 | intron variant | T/G | snv | 0.91 | 5 | |||
rs5993499 | 1.000 | 22 | 16587858 | downstream gene variant | C/T | snv | 6.8E-02 | 5 | |||
rs718084 | 1.000 | 6 | 166681163 | intron variant | C/T | snv | 0.42 | 5 | |||
rs552304070 | 1.000 | 1 | 167426238 | 3 prime UTR variant | AAA/-;A;AA;AAAA;AAAAAAAAA | delins | 4.6E-02 | 5 | |||
rs10039039 | 1.000 | 5 | 170487960 | intron variant | C/T | snv | 8.9E-02 | 5 | |||
rs17079875 | 1.000 | 5 | 179974542 | intron variant | G/A | snv | 6.8E-02 | 5 |