Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8061882 | 0.827 | 0.120 | 16 | 11067551 | intron variant | G/C | snv | 0.11 | 5 | ||
rs35441874 | 0.882 | 0.120 | 16 | 11119164 | intron variant | T/A | snv | 0.19 | 3 | ||
rs36045143 | 1.000 | 0.080 | 16 | 11131109 | intron variant | A/G | snv | 0.18 | 3 | ||
rs12935657 | 0.925 | 0.080 | 16 | 11125184 | intron variant | G/A | snv | 0.18 | 2 | ||
rs12924729 | 0.882 | 0.200 | 16 | 11093926 | intron variant | G/A | snv | 0.34 | 2 | ||
rs12927355 | 0.882 | 0.240 | 16 | 11100914 | intron variant | C/A;T | snv | 0.29 | 2 | ||
rs34972832 | 0.925 | 0.120 | 16 | 11105081 | intron variant | G/A;T | snv | 0.14 | 2 | ||
rs7200786 | 0.882 | 0.200 | 16 | 11083944 | intron variant | A/G | snv | 0.59 | 2 | ||
rs34069391 | 0.925 | 0.080 | 16 | 11067358 | intron variant | T/- | delins | 2 | |||
rs12935413 | 1.000 | 0.080 | 16 | 11116590 | intron variant | G/A | snv | 0.34 | 2 | ||
rs35032408 | 0.925 | 0.080 | 16 | 11121567 | intron variant | T/C;G | snv | 2 | |||
rs11644510 | 1.000 | 0.120 | 16 | 11183501 | downstream gene variant | C/T | snv | 0.39 | 2 | ||
rs11645657 | 1.000 | 0.080 | 16 | 11129597 | intron variant | C/A;G | snv | 0.48 | 2 | ||
rs7203459 | 1.000 | 0.080 | 16 | 11136846 | intron variant | T/C | snv | 0.23 | 2 | ||
rs62026376 | 0.925 | 0.120 | 16 | 11134855 | intron variant | C/T | snv | 0.18 | 2 | ||
rs3862469 | 1.000 | 0.040 | 16 | 11100223 | intron variant | C/T | snv | 0.35 | 1 | ||
rs17806299 | 1.000 | 0.080 | 16 | 11106123 | intron variant | G/A | snv | 0.15 | 1 | ||
rs9923856 | 1.000 | 0.080 | 16 | 11116558 | intron variant | T/C | snv | 0.41 | 1 | ||
rs12708715 | 1.000 | 0.080 | 16 | 11083967 | intron variant | C/T | snv | 0.39 | 1 | ||
rs725613 | 0.851 | 0.240 | 16 | 11075826 | intron variant | T/G | snv | 0.42 | 1 | ||
rs2903692 | 0.807 | 0.360 | 16 | 11144926 | intron variant | G/A | snv | 0.33 | 1 | ||
rs12708716 | 0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 | 1 | ||
rs887864 | 0.925 | 0.120 | 16 | 11065028 | intron variant | G/A;C;T | snv | 1 | |||
rs248831 | 16 | 11187361 | intergenic variant | G/A | snv | 0.31 | 1 | ||||
rs2041670 | 0.851 | 0.280 | 16 | 11080795 | intron variant | G/A;C | snv | 1 |