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 | |||
rs1333040 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 15 | |||
rs1537372 | 0.752 | 0.120 | 9 | 22103184 | intron variant | G/A;T | snv | 14 | |||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 14 | |||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 13 | |||
rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 11 | |||
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 10 | |||
rs751093906 | 0.882 | 0.200 | 8 | 42472255 | stop gained | G/A;C | snv | 4.0E-06 | 8 | ||
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 | |||
rs9632884 | 0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv | 6 | |||
rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
rs3218020 | 0.882 | 0.120 | 9 | 21997873 | intron variant | G/A;C | snv | 5 | |||
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
rs1440581 | 1.000 | 0.080 | 4 | 88305270 | intron variant | T/A;C | snv | 4 | |||
rs1912826 | 4 | 186228386 | intron variant | G/A;C | snv | 4 | |||||
rs7857345 | 0.925 | 0.080 | 9 | 22087474 | non coding transcript exon variant | T/A;C | snv | 4 | |||
rs944801 | 0.882 | 0.120 | 9 | 22051671 | intron variant | G/A;C | snv | 4 | |||
rs1004638 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 3 | |||
rs10738605 | 0.925 | 0.120 | 9 | 22049131 | non coding transcript exon variant | C/A;G | snv | 3 | |||
rs10738609 | 1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv | 3 | |||
rs10811647 | 1.000 | 0.040 | 9 | 22065003 | intron variant | C/G;T | snv | 3 | |||
rs10965212 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 3 |