Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13447 | 0.882 | 0.200 | 7 | 75166663 | non coding transcript exon variant | T/A;C | snv | 1.9E-02 | 4 | ||
rs17581834 | 0.882 | 0.120 | 1 | 206802774 | intron variant | T/C | snv | 4.2E-02 | 3 | ||
rs201802880 | 0.882 | 0.200 | 7 | 74779296 | missense variant | G/A | snv | 1.1E-03 | 4 | ||
rs2242665 | 0.882 | 0.160 | 6 | 31871532 | missense variant | C/T | snv | 0.60 | 0.60 | 3 | |
rs2248932 | 0.882 | 0.160 | 8 | 11534141 | intron variant | A/G | snv | 0.60 | 3 | ||
rs2283790 | 0.882 | 0.120 | 22 | 21602364 | intron variant | A/G | snv | 0.21 | 3 | ||
rs2377422 | 0.882 | 0.200 | 12 | 8128312 | intron variant | C/T | snv | 0.60 | 3 | ||
rs2596501 | 0.882 | 0.200 | 6 | 31353434 | intron variant | C/T | snv | 0.57 | 3 | ||
rs2844635 | 0.882 | 0.200 | 6 | 31107704 | downstream gene variant | A/G | snv | 0.37 | 3 | ||
rs3844283 | 0.882 | 0.200 | 3 | 10222796 | missense variant | C/G | snv | 0.37 | 0.35 | 3 | |
rs3890733 | 0.882 | 0.120 | 12 | 47895590 | intron variant | C/T | snv | 0.27 | 3 | ||
rs437179 | 0.882 | 0.160 | 6 | 31961237 | missense variant | A/C | snv | 0.76 | 0.78 | 3 | |
rs4937333 | 0.882 | 0.120 | 11 | 128460625 | 3 prime UTR variant | T/C | snv | 0.45 | 4 | ||
rs5029937 | 0.882 | 0.160 | 6 | 137874014 | intron variant | G/T | snv | 0.13 | 4 | ||
rs535586 | 0.882 | 0.160 | 6 | 31892560 | splice region variant | T/A;C | snv | 0.77 | 3 | ||
rs644827 | 0.882 | 0.160 | 6 | 31870664 | missense variant | T/C | snv | 0.60 | 0.60 | 3 | |
rs6457536 | 0.882 | 0.200 | 6 | 32305988 | intron variant | A/G | snv | 0.21 | 3 | ||
rs659445 | 0.882 | 0.160 | 6 | 31896527 | intron variant | G/A;C | snv | 0.77 | 0.76 | 3 | |
rs660550 | 0.882 | 0.160 | 6 | 31869500 | intron variant | C/A;G | snv | 0.60 | 3 | ||
rs7579944 | 0.882 | 0.200 | 2 | 30222160 | intergenic variant | T/C;G | snv | 5 | |||
rs7745656 | 0.882 | 0.200 | 6 | 32713193 | upstream gene variant | G/T | snv | 0.29 | 3 | ||
rs7758736 | 0.882 | 0.200 | 6 | 32790617 | intergenic variant | G/A | snv | 0.14 | 3 | ||
rs799454 | 0.882 | 0.200 | 14 | 34927973 | intron variant | A/G | snv | 0.45 | 3 | ||
rs878081 | 0.882 | 0.200 | 21 | 44288394 | synonymous variant | C/T | snv | 0.21 | 0.19 | 3 | |
rs922483 | 0.882 | 0.200 | 8 | 11494403 | 5 prime UTR variant | C/T | snv | 0.31 | 3 |