Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 8 | |||
rs56113850 | 0.807 | 0.080 | 19 | 40847202 | intron variant | T/C | snv | 0.52 | 8 | ||
rs112635299 | 1.000 | 0.040 | 14 | 94371805 | downstream gene variant | G/T | snv | 1.3E-02 | 7 | ||
rs55781567 | 0.851 | 0.080 | 15 | 78565644 | 5 prime UTR variant | C/G | snv | 0.31 | 7 | ||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 6 | |
rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 6 | ||
rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 6 | ||
rs9788721 | 1.000 | 0.040 | 15 | 78510527 | intron variant | C/T | snv | 0.65 | 6 | ||
rs138544659 | 1.000 | 0.040 | 15 | 78608359 | intron variant | T/G | snv | 0.28 | 5 | ||
rs190065944 | 0.925 | 0.080 | 15 | 78567268 | intron variant | G/A | snv | 3.4E-03 | 5 | ||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 5 | ||
rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 5 | ||
rs55958997 | 1.000 | 0.040 | 15 | 78623530 | upstream gene variant | C/A | snv | 0.32 | 5 | ||
rs7655625 | 1.000 | 0.040 | 4 | 144564763 | intron variant | T/C;G | snv | 5 | |||
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 5 | |
rs8042374 | 0.807 | 0.200 | 15 | 78615690 | intron variant | A/G | snv | 0.29 | 5 | ||
rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 4 | ||
rs10851907 | 1.000 | 0.040 | 15 | 78623522 | upstream gene variant | G/A | snv | 0.40 | 4 | ||
rs11639372 | 0.925 | 0.080 | 15 | 78674313 | intron variant | C/T | snv | 0.30 | 4 | ||
rs117068593 | 14 | 92651884 | missense variant | C/T | snv | 0.13 | 0.11 | 4 | |||
rs12504628 | 1.000 | 0.040 | 4 | 144515172 | intron variant | T/C | snv | 0.33 | 4 | ||
rs12902602 | 15 | 78675059 | intron variant | A/G | snv | 0.28 | 4 | ||||
rs13116999 | 4 | 144521212 | intron variant | G/A | snv | 0.65 | 4 | ||||
rs17486278 | 0.827 | 0.120 | 15 | 78575140 | intron variant | A/C | snv | 0.32 | 4 |