Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10849433 | 0.776 | 0.080 | 12 | 6297738 | regulatory region variant | T/C | snv | 0.38 | 10 | ||
rs10980628 | 0.776 | 0.080 | 9 | 110909123 | intron variant | T/C | snv | 0.16 | 10 | ||
rs11085466 | 0.790 | 0.080 | 19 | 21569009 | intron variant | G/C | snv | 0.23 | 10 | ||
rs11087784 | 0.776 | 0.080 | 20 | 7760329 | intergenic variant | A/G | snv | 0.13 | 10 | ||
rs11150038 | 0.790 | 0.080 | 16 | 78042662 | intron variant | A/C;G | snv | 10 | |||
rs11169552 | 0.776 | 0.080 | 12 | 50761880 | upstream gene variant | C/T | snv | 0.23 | 10 | ||
rs11190164 | 0.776 | 0.080 | 10 | 99591947 | intergenic variant | A/G | snv | 0.19 | 10 | ||
rs11196170 | 0.776 | 0.080 | 10 | 112962862 | intron variant | G/A;C | snv | 10 | |||
rs11610543 | 0.776 | 0.080 | 12 | 42740389 | intergenic variant | A/G;T | snv | 10 | |||
rs116353863 | 0.776 | 0.080 | 6 | 31042408 | regulatory region variant | T/C | snv | 2.2E-02 | 10 | ||
rs11692435 | 0.790 | 0.080 | 2 | 97658891 | missense variant | G/A | snv | 7.0E-02 | 6.7E-02 | 10 | |
rs117079142 | 0.776 | 0.080 | 8 | 116778675 | intron variant | C/A | snv | 3.0E-02 | 10 | ||
rs11884596 | 0.776 | 0.080 | 2 | 198747683 | intron variant | T/C | snv | 0.32 | 10 | ||
rs12144319 | 0.776 | 0.080 | 1 | 54780362 | 3 prime UTR variant | T/C | snv | 0.31 | 10 | ||
rs12149163 | 0.776 | 0.080 | 16 | 86305709 | upstream gene variant | T/C | snv | 0.49 | 10 | ||
rs12246635 | 0.776 | 0.080 | 10 | 112528860 | intron variant | T/C | snv | 0.13 | 10 | ||
rs12372718 | 0.776 | 0.080 | 12 | 50777307 | intron variant | A/G | snv | 0.35 | 10 | ||
rs12447408 | 0.776 | 0.080 | 16 | 86218938 | downstream gene variant | G/A | snv | 0.21 | 10 | ||
rs1250567 | 0.776 | 0.080 | 10 | 79286508 | intron variant | T/C | snv | 0.56 | 10 | ||
rs12514517 | 0.776 | 0.080 | 5 | 40279974 | intergenic variant | G/A | snv | 0.21 | 10 | ||
rs12594720 | 0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 | 10 | ||
rs12646351 | 0.790 | 0.080 | 4 | 145819473 | intron variant | G/A | snv | 0.19 | 10 | ||
rs12672022 | 0.776 | 0.080 | 7 | 45096824 | downstream gene variant | T/C | snv | 0.13 | 10 | ||
rs12708491 | 0.776 | 0.080 | 15 | 32700635 | downstream gene variant | G/A | snv | 0.33 | 10 | ||
rs13086367 | 0.776 | 0.080 | 3 | 113185041 | downstream gene variant | A/G | snv | 0.38 | 10 |