Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4977574 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 26 | |||
rs1063192 | 0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv | 24 | |||
rs4977756 | 0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 | 24 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 | ||
rs3217992 | 0.683 | 0.480 | 9 | 22003224 | 3 prime UTR variant | C/T | snv | 0.32 | 22 | ||
rs564398 | 0.716 | 0.360 | 9 | 22029548 | 3 prime UTR variant | T/C | snv | 0.31 | 0.28 | 18 | |
rs2157719 | 0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 | 17 | ||
rs1333040 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 15 | |||
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 11 | |||
rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 7 | ||
rs523096 | 0.827 | 0.080 | 9 | 22019130 | intron variant | A/G | snv | 0.30 | 7 | ||
rs7049105 | 0.807 | 0.120 | 9 | 22028802 | intron variant | A/G | snv | 0.58 | 7 | ||
rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
rs2383204 | 0.827 | 0.160 | 9 | 22055049 | intron variant | A/G;T | snv | 6 | |||
rs496892 | 0.827 | 0.160 | 9 | 22024352 | intron variant | C/T | snv | 0.40 | 6 | ||
rs634537 | 0.851 | 0.080 | 9 | 22032153 | intron variant | T/G | snv | 0.28 | 6 | ||
rs9632884 | 0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv | 6 | |||
rs10811650 | 0.882 | 0.200 | 9 | 22067594 | intron variant | A/G | snv | 0.37 | 5 | ||
rs3218020 | 0.882 | 0.120 | 9 | 21997873 | intron variant | G/A;C | snv | 5 | |||
rs944797 | 0.882 | 0.120 | 9 | 22115287 | intron variant | T/C;G | snv | 0.49 | 5 | ||
rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
rs10965215 | 0.882 | 0.120 | 9 | 22029446 | missense variant | G/A | snv | 0.55 | 0.46 | 4 | |
rs10965219 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 4 |