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 | |||
rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
rs10738607 | 0.925 | 0.080 | 9 | 22088095 | intron variant | A/G | snv | 0.42 | 4 | ||
rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
rs10757264 | 1.000 | 0.040 | 9 | 22019733 | intron variant | A/G | snv | 0.58 | 2 | ||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs10811656 | 0.807 | 0.200 | 9 | 22124473 | intron variant | C/T | snv | 0.47 | 7 | ||
rs10965212 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 3 | |||
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 | ||
rs1333040 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 15 | |||
rs1333042 | 0.827 | 0.120 | 9 | 22103814 | intron variant | A/G | snv | 0.63 | 7 | ||
rs1333045 | 0.776 | 0.280 | 9 | 22119196 | non coding transcript exon variant | T/C | snv | 0.50 | 14 | ||
rs1333047 | 0.790 | 0.240 | 9 | 22124505 | intron variant | A/T | snv | 0.63 | 9 | ||
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 24 | ||
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
rs1537372 | 0.752 | 0.120 | 9 | 22103184 | intron variant | G/A;T | snv | 14 | |||
rs1537374 | 1.000 | 0.040 | 9 | 22116047 | intron variant | A/G | snv | 0.64 | 3 | ||
rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
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 | ||
rs2383206 | 0.742 | 0.320 | 9 | 22115027 | intron variant | A/G | snv | 0.49 | 17 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 |