Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3194051 | 0.851 | 0.200 | 5 | 35876172 | missense variant | A/G | snv | 0.24 | 0.28 | 4 | |
rs10336 | 0.851 | 0.240 | 4 | 76001835 | 3 prime UTR variant | A/G;T | snv | 4 | |||
rs13412852 | 0.851 | 0.120 | 2 | 11774815 | intron variant | C/T | snv | 0.26 | 4 | ||
rs4619915 | 0.882 | 0.120 | 4 | 76034048 | 3 prime UTR variant | A/G | snv | 0.61 | 3 | ||
rs3741981 | 0.882 | 0.120 | 12 | 112911065 | missense variant | G/A;C | snv | 3 | |||
rs17886084 | 1.000 | 0.080 | 11 | 102799765 | intron variant | C/- | delins | 2 | |||
rs267607117 | 0.925 | 0.080 | 8 | 93780747 | missense variant | G/T | snv | 2 | |||
rs1063303 | 0.925 | 0.120 | 11 | 5698520 | missense variant | G/A;C;T | snv | 4.0E-06; 0.50; 1.6E-05 | 2 | ||
rs9402373 | 1.000 | 0.080 | 6 | 131956291 | intron variant | C/A;G;T | snv | 1 | |||
rs900837802 | 1.000 | 0.080 | 2 | 88595498 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs5496 | 1.000 | 0.080 | 19 | 10284771 | intron variant | G/A | snv | 7.8E-03 | 3.3E-02 | 1 | |
rs1430059719 | 1.000 | 0.080 | 20 | 46012456 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs781521972 | 1.000 | 0.080 | 18 | 47896706 | synonymous variant | T/A | snv | 4.0E-06 | 1 | ||
rs1060500764 | 1.000 | 0.080 | 15 | 67181363 | missense variant | A/G | snv | 1 |