Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7768897 | 0.925 | 0.080 | 6 | 110891080 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs1400295986 | 0.925 | 0.080 | 5 | 112838233 | missense variant | T/C | snv | 2 | |||
rs28933379 | 1.000 | 0.080 | 5 | 112838953 | missense variant | G/A | snv | 2 | |||
rs2279284 | 0.925 | 0.080 | 11 | 13277203 | intron variant | C/T | snv | 0.25 | 2 | ||
rs911160 | 0.925 | 0.080 | 20 | 56382507 | intron variant | G/A;C | snv | 2 | |||
rs2241909 | 0.925 | 0.080 | 17 | 8205021 | synonymous variant | G/A | snv | 0.66 | 0.64 | 2 | |
rs2289590 | 0.925 | 0.080 | 17 | 8207446 | intron variant | C/A | snv | 0.54 | 2 | ||
rs11084490 | 0.925 | 0.080 | 19 | 57231104 | 5 prime UTR variant | G/A;C;T | snv | 0.87; 3.8E-05 | 2 | ||
rs758099 | 0.925 | 0.080 | 19 | 57231966 | intron variant | C/G;T | snv | 2 | |||
rs1044432 | 0.925 | 0.080 | 11 | 13388251 | 3 prime UTR variant | A/T | snv | 0.16 | 2 | ||
rs384490 | 0.925 | 0.080 | 11 | 3057655 | splice region variant | T/G | snv | 0.46 | 2 | ||
rs729662 | 0.925 | 0.080 | 11 | 3006910 | synonymous variant | G/A | snv | 0.35 | 0.25 | 2 | |
rs7394702 | 0.925 | 0.080 | 11 | 3022918 | intron variant | T/C | snv | 0.17 | 2 | ||
rs121909776 | 1.000 | 0.080 | 2 | 201187798 | missense variant | T/C | snv | 1.2E-04 | 2.8E-05 | 2 | |
rs4647693 | 0.925 | 0.080 | 4 | 184629610 | intron variant | T/C | snv | 0.31 | 2 | ||
rs10787498 | 0.925 | 0.080 | 10 | 113729891 | 3 prime UTR variant | T/G | snv | 0.38 | 2 | ||
rs1127687 | 0.925 | 0.080 | 10 | 113730350 | 3 prime UTR variant | G/A | snv | 0.23 | 2 | ||
rs12247479 | 0.925 | 0.080 | 10 | 113730301 | 3 prime UTR variant | G/A | snv | 0.16 | 2 | ||
rs746782366 | 0.925 | 0.120 | 21 | 43072117 | missense variant | C/G;T | snv | 8.1E-06; 4.0E-06 | 2 | ||
rs77447679 | 0.925 | 0.080 | 17 | 79836675 | intron variant | C/A | snv | 5.4E-02 | 2 | ||
rs17690554 | 0.925 | 0.080 | 16 | 68835607 | downstream gene variant | C/G;T | snv | 2 | |||
rs11133399 | 0.925 | 0.080 | 4 | 55547664 | non coding transcript exon variant | A/G | snv | 0.28 | 2 | ||
rs11170877 | 0.925 | 0.080 | 12 | 54340505 | start lost | A/G | snv | 0.16 | 0.17 | 2 | |
rs12231393 | 0.925 | 0.080 | 12 | 54318989 | intron variant | T/C | snv | 0.14 | 2 | ||
rs7208768 | 0.925 | 0.080 | 17 | 1449407 | intron variant | G/A | snv | 0.56 | 2 |