Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7632500 | 0.925 | 0.080 | 3 | 168007561 | downstream gene variant | A/G | snv | 0.17 | 5 | ||
rs764643047 | 0.851 | 0.120 | 3 | 9750336 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
rs4676893 | 0.882 | 0.080 | 3 | 70868488 | intergenic variant | A/T | snv | 0.61 | 3 | ||
rs11901649 | 0.882 | 0.080 | 2 | 21027351 | intron variant | G/A;C;T | snv | 3 | |||
rs7255 | 0.925 | 0.080 | 2 | 20679060 | 3 prime UTR variant | T/A;C | snv | 3 | |||
rs1247942 | 0.925 | 0.080 | 12 | 114235918 | downstream gene variant | G/A;C | snv | 2 | |||
rs1979654 | 0.925 | 0.080 | 16 | 86363229 | TF binding site variant | G/C | snv | 0.55 | 2 | ||
rs2687202 | 0.925 | 0.080 | 3 | 70880832 | regulatory region variant | T/C | snv | 0.64 | 2 | ||
rs2701108 | 0.925 | 0.160 | 12 | 114236456 | downstream gene variant | T/C | snv | 0.35 | 2 | ||
rs62423175 | 0.925 | 0.080 | 6 | 61485463 | intergenic variant | G/A | snv | 2 | |||
rs9823696 | 0.925 | 0.080 | 3 | 184065565 | downstream gene variant | A/G;T | snv | 2 | |||
rs491603 | 1.000 | 0.080 | 1 | 36066715 | 3 prime UTR variant | T/A;C | snv | 2 | |||
rs2518720 | 0.925 | 0.080 | 9 | 21978980 | intron variant | C/T | snv | 0.43 | 2 | ||
rs9918259 | 0.925 | 0.080 | 5 | 662977 | 3 prime UTR variant | C/T | snv | 2.1E-03 | 2 | ||
rs17451754 | 0.925 | 0.080 | 7 | 117616658 | intron variant | G/A | snv | 0.10 | 2 | ||
rs199620551 | 0.925 | 0.080 | 19 | 18693485 | intron variant | G/- | del | 9.2E-02 | 2 | ||
rs3072 | 0.925 | 0.160 | 2 | 20678646 | 3 prime UTR variant | T/C | snv | 0.30 | 2 | ||
rs10108511 | 0.925 | 0.080 | 8 | 11578007 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs2464469 | 0.925 | 0.080 | 15 | 58069827 | intron variant | G/A | snv | 0.65 | 2 | ||
rs17749155 | 0.925 | 0.080 | 8 | 10210563 | intron variant | G/A | snv | 0.16 | 2 | ||
rs7852462 | 0.925 | 0.080 | 9 | 97548219 | intron variant | C/A;T | snv | 2 | |||
rs1263178238 | 0.925 | 0.080 | 19 | 51338047 | missense variant | T/C | snv | 2.6E-05 | 4.9E-05 | 2 | |
rs2671828 | 1.000 | 0.080 | 17 | 35404745 | upstream gene variant | T/C | snv | 0.55 | 1 | ||
rs3776082 | 1.000 | 0.080 | 5 | 150164482 | upstream gene variant | G/A;C | snv | 1 | |||
rs4769585 | 1.000 | 0.080 | 13 | 27976441 | downstream gene variant | C/T | snv | 0.39 | 1 |