Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7533564 | 0.925 | 0.120 | 1 | 78360228 | intron variant | C/T | snv | 0.92 | 4 | ||
rs1233478 | 0.925 | 0.120 | 6 | 29510044 | intron variant | G/A;C;T | snv | 3 | |||
rs1264622 | 1.000 | 0.120 | 6 | 30289159 | non coding transcript exon variant | C/T | snv | 0.13 | 3 | ||
rs13422767 | 0.882 | 0.120 | 2 | 162243749 | intron variant | G/A | snv | 0.14 | 3 | ||
rs17533090 | 1.000 | 0.120 | 6 | 32622945 | TF binding site variant | G/T | snv | 0.16 | 3 | ||
rs3130048 | 1.000 | 0.120 | 6 | 31645962 | intron variant | T/C | snv | 0.23 | 3 | ||
rs3842727 | 1.000 | 0.120 | 11 | 2163618 | upstream gene variant | G/T | snv | 0.58 | 3 | ||
rs428595 | 1.000 | 0.120 | 22 | 21662102 | non coding transcript exon variant | A/G | snv | 0.98 | 3 | ||
rs6476839 | 0.925 | 0.120 | 9 | 4290823 | intron variant | A/C;T | snv | 3 | |||
rs7171171 | 0.925 | 0.120 | 15 | 38614840 | intergenic variant | A/G | snv | 0.24 | 3 | ||
rs754855896 | 0.925 | 0.120 | 6 | 32758877 | missense variant | G/A;T | snv | 4.0E-06; 8.1E-06 | 3 | ||
rs927292 | 1.000 | 0.120 | 14 | 68792124 | intron variant | C/G | snv | 0.68 | 3 | ||
rs9273368 | 0.882 | 0.120 | 6 | 32658698 | upstream gene variant | G/A | snv | 0.23 | 3 | ||
rs9273643 | 0.925 | 0.120 | 6 | 32661407 | missense variant | A/G | snv | 3 | |||
rs1015166 | 0.925 | 0.120 | 6 | 32830954 | intron variant | C/G;T | snv | 0.28 | 2 | ||
rs10766196 | 0.925 | 0.120 | 11 | 14891585 | 5 prime UTR variant | A/G | snv | 0.35 | 2 | ||
rs10770141 | 1.000 | 0.120 | 11 | 2172610 | upstream gene variant | A/C;G | snv | 2 | |||
rs10914542 | 0.925 | 0.120 | 1 | 32262639 | intron variant | C/G | snv | 0.15 | 2 | ||
rs1131568 | 1.000 | 0.120 | 3 | 172505900 | 3 prime UTR variant | T/C | snv | 0.70 | 2 | ||
rs11575248 | 1.000 | 0.120 | 12 | 56342206 | 3 prime UTR variant | G/T | snv | 4.5E-02 | 2 | ||
rs1223438908 | 1.000 | 0.120 | 3 | 105681480 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs13330041 | 1.000 | 0.120 | 16 | 10994951 | intron variant | G/A | snv | 0.25 | 2 | ||
rs1358030 | 0.925 | 0.120 | 10 | 106363841 | intergenic variant | G/A | snv | 0.57 | 2 | ||
rs140101069 | 1.000 | 0.120 | 9 | 3828342 | missense variant | G/A | snv | 3.2E-04 | 8.4E-05 | 2 | |
rs1419675 | 1.000 | 0.120 | 6 | 30124930 | intergenic variant | G/T | snv | 0.74 | 2 |