Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10008637 | 4 | 76492991 | intron variant | T/A;C | snv | 0.35 | 2 | ||||
rs1010553 | 1.000 | 0.080 | 3 | 52506757 | synonymous variant | T/C | snv | 0.53 | 0.59 | 2 | |
rs10168349 | 2 | 46133768 | intron variant | G/C | snv | 0.36 | 4 | ||||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 12 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 9 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 25 | ||
rs10495928 | 2 | 46126027 | intron variant | A/G | snv | 0.36 | 5 | ||||
rs10711289 | 3 | 169450583 | intron variant | AAA/-;A;AA;AAAA;AAAAA | delins | 1 | |||||
rs10901252 | 9 | 133252613 | non coding transcript exon variant | G/C | snv | 0.11 | 3 | ||||
rs10953299 | 7 | 100645788 | intron variant | T/C | snv | 0.21 | 1 | ||||
rs11039436 | 11 | 47866484 | intergenic variant | A/C;G;T | snv | 2 | |||||
rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 17 | ||
rs11072566 | 0.925 | 0.120 | 15 | 76001630 | intron variant | A/G | snv | 0.45 | 5 | ||
rs11072567 | 15 | 76006403 | intron variant | A/G | snv | 0.43 | 5 | ||||
rs111843364 | 16 | 70923707 | intron variant | G/A | snv | 3.8E-02 | 1 | ||||
rs112682076 | 1 | 10297748 | intron variant | G/C | snv | 5.8E-03 | 2 | ||||
rs114948639 | 2 | 46066687 | intron variant | C/T | snv | 7.2E-03 | 3 | ||||
rs115986297 | 6 | 2050557 | intron variant | A/C;G | snv | 3 | |||||
rs11654074 | 17 | 59748211 | intron variant | A/C | snv | 0.40 | 5 | ||||
rs11665867 | 19 | 40760574 | intron variant | A/G | snv | 0.13 | 1 | ||||
rs11689538 | 2 | 121238062 | intron variant | G/C | snv | 0.11 | 3 | ||||
rs11730623 | 4 | 69020433 | upstream gene variant | A/T | snv | 0.66 | 2 | ||||
rs11760376 | 7 | 134684558 | intron variant | A/G | snv | 1.9E-03 | 2 | ||||
rs12310617 | 0.851 | 0.120 | 12 | 3060327 | intergenic variant | C/T | snv | 0.11 | 16 | ||
rs12369179 | 0.851 | 0.120 | 12 | 122479003 | intron variant | C/T | snv | 5.9E-02 | 16 |