Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1004638 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 3 | |||
rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
rs10965212 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 3 | |||
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 | |||
rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 10 | |||
rs4977574 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 26 | |||
rs4977575 | 1.000 | 0.040 | 9 | 22124745 | intron variant | C/G;T | snv | 2 | |||
rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 11 | |||
rs9632884 | 0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv | 6 | |||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
rs564398 | 0.716 | 0.360 | 9 | 22029548 | 3 prime UTR variant | T/C | snv | 0.31 | 0.28 | 18 | |
rs523096 | 0.827 | 0.080 | 9 | 22019130 | intron variant | A/G | snv | 0.30 | 7 | ||
rs9349379 | 0.732 | 0.200 | 6 | 12903725 | intron variant | A/G | snv | 0.32 | 19 | ||
rs3217992 | 0.683 | 0.480 | 9 | 22003224 | 3 prime UTR variant | C/T | snv | 0.32 | 22 | ||
rs173539 | 0.882 | 0.080 | 16 | 56954132 | intergenic variant | C/T | snv | 0.33 | 11 | ||
rs2026458 | 0.882 | 0.080 | 6 | 12825642 | intron variant | C/T | snv | 0.34 | 6 | ||
rs496892 | 0.827 | 0.160 | 9 | 22024352 | intron variant | C/T | snv | 0.40 | 6 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs2891168 | 0.851 | 0.160 | 9 | 22098620 | intron variant | A/G | snv | 0.40 | 5 | ||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs10738607 | 0.925 | 0.080 | 9 | 22088095 | intron variant | A/G | snv | 0.42 | 4 |