Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1966862 | 0.790 | 0.120 | 4 | 85766908 | intron variant | A/G | snv | 0.14 | 8 | ||
rs200378616 | 0.882 | 0.120 | 7 | 87544938 | missense variant | G/C;T | snv | 4.0E-05; 8.0E-06 | 3 | ||
rs2274407 | 0.882 | 0.120 | 13 | 95206781 | missense variant | C/A;G;T | snv | 9.7E-02 | 0.10 | 4 | |
rs2413739 | 0.827 | 0.120 | 22 | 43001030 | intron variant | C/T | snv | 0.43 | 6 | ||
rs2742038 | 0.882 | 0.120 | 10 | 101137330 | 3 prime UTR variant | C/T | snv | 0.16 | 3 | ||
rs35134728 | 0.882 | 0.120 | 1 | 11787277 | 3 prime UTR variant | -/AGA | delins | 3 | |||
rs368005287 | 0.882 | 0.120 | 7 | 99762071 | stop gained | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
rs3731246 | 0.882 | 0.120 | 9 | 21971990 | intron variant | C/G | snv | 0.11 | 3 | ||
rs3737966 | 0.882 | 0.120 | 1 | 11787702 | 3 prime UTR variant | C/T | snv | 0.55 | 3 | ||
rs3758149 | 0.882 | 0.120 | 8 | 63039169 | upstream gene variant | G/A | snv | 0.24 | 3 | ||
rs3794012 | 0.882 | 0.120 | 11 | 8248697 | intron variant | T/C | snv | 0.32 | 3 | ||
rs41320251 | 0.882 | 0.120 | 20 | 3213196 | missense variant | C/A;G | snv | 3 | |||
rs414580 | 0.882 | 0.120 | 8 | 16177793 | intron variant | T/A;C | snv | 3 | |||
rs4149009 | 0.882 | 0.120 | 12 | 21267537 | 3 prime UTR variant | C/T | snv | 0.38 | 3 | ||
rs4237770 | 0.882 | 0.120 | 11 | 8254288 | intron variant | T/C | snv | 0.37 | 3 | ||
rs442264 | 0.882 | 0.120 | 11 | 8242602 | intron variant | G/A | snv | 0.44 | 3 | ||
rs4646450 | 0.882 | 0.120 | 7 | 99668695 | 3 prime UTR variant | G/A | snv | 0.38 | 4 | ||
rs4748793 | 0.851 | 0.120 | 10 | 22194082 | intergenic variant | A/G | snv | 0.18 | 4 | ||
rs525549 | 0.882 | 0.120 | 11 | 118487353 | intron variant | T/A | snv | 0.33 | 3 | ||
rs57725551 | 0.882 | 0.120 | 21 | 45525868 | synonymous variant | G/T | snv | 5.3E-03 | 7.0E-03 | 3 | |
rs6021191 | 0.851 | 0.120 | 20 | 51419700 | intron variant | A/T | snv | 4.9E-02 | 5 | ||
rs62571442 | 0.882 | 0.120 | 9 | 134850278 | non coding transcript exon variant | G/A;C;T | snv | 0.58; 4.4E-03 | 3 | ||
rs6461639 | 0.882 | 0.120 | 7 | 22147337 | intron variant | T/A;C | snv | 3 | |||
rs6589664 | 0.882 | 0.120 | 11 | 118534089 | synonymous variant | G/A | snv | 0.30 | 0.27 | 3 | |
rs6964969 | 0.851 | 0.120 | 7 | 50405553 | downstream gene variant | A/G | snv | 0.23 | 4 |