Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2392929 | 7 | 106773623 | upstream gene variant | T/A;C;G | snv | 4 | |||||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 10 | |||
rs2932538 | 1 | 112673921 | intron variant | A/C;G | snv | 4 | |||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs35441 | 12 | 115115310 | intergenic variant | C/T | snv | 0.40 | 5 | ||||
rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
rs3774372 | 1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 | 4 | |
rs381815 | 1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 | 6 | ||
rs419076 | 3 | 169383098 | intron variant | T/A;C | snv | 6 | |||||
rs4373814 | 10 | 18131043 | intergenic variant | G/C;T | snv | 5 | |||||
rs438885 | 2 | 164195781 | intron variant | A/T | snv | 0.56 | 5 | ||||
rs4590817 | 10 | 61707795 | intron variant | G/C | snv | 0.15 | 5 | ||||
rs6015450 | 20 | 59176062 | intron variant | A/G | snv | 0.14 | 7 | ||||
rs62434109 | 6 | 150654176 | intron variant | T/G | snv | 8.4E-02 | 5 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs7129220 | 11 | 10328991 | intron variant | G/A | snv | 0.10 | 5 | ||||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs7823056 | 8 | 8525195 | intergenic variant | A/G | snv | 0.55 | 3 | ||||
rs805303 | 0.925 | 0.160 | 6 | 31648589 | intron variant | G/A | snv | 0.45 | 7 | ||
rs932764 | 10 | 94136183 | intron variant | A/G | snv | 0.38 | 6 | ||||
rs5883070 | 7 | 27240226 | intron variant | -/AAAACA;AACA | delins | 0.91 | 5 |