Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | ||
rs34933034 | 0.925 | 0.120 | 15 | 74787133 | intron variant | G/A;T | snv | 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 | |
rs494620 | 0.925 | 0.120 | 6 | 31870936 | stop gained | G/A;T | snv | 0.44; 4.1E-06 | 3 | ||
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 | ||
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 | ||
rs9267531 | 0.882 | 0.120 | 6 | 31668965 | non coding transcript exon variant | A/G | snv | 7.5E-02 | 3 | ||
rs10954214 | 0.851 | 0.160 | 7 | 128949579 | 3 prime UTR variant | C/T | snv | 0.64 | 4 | ||
rs11085725 | 0.851 | 0.160 | 19 | 10351837 | intron variant | C/T | snv | 0.24 | 4 | ||
rs112846137 | 0.851 | 0.160 | 3 | 160595133 | intergenic variant | G/T | snv | 5.3E-02 | 4 | ||
rs1217393 | 0.851 | 0.160 | 1 | 113891324 | intron variant | G/A | snv | 0.42 | 4 | ||
rs13389408 | 0.851 | 0.160 | 2 | 191068557 | 3 prime UTR variant | T/C | snv | 7.4E-02 | 4 | ||
rs13447 | 0.882 | 0.200 | 7 | 75166663 | non coding transcript exon variant | T/A;C | snv | 1.9E-02 | 4 |