Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs759412116 | 0.581 | 0.640 | 19 | 45352210 | missense variant | C/G;T | snv | 4.0E-06; 6.0E-05 | 55 | ||
rs2297518 | 0.658 | 0.480 | 17 | 27769571 | missense variant | G/A | snv | 0.18 | 0.17 | 30 | |
rs3088440 | 0.776 | 0.240 | 9 | 21968160 | 3 prime UTR variant | G/A | snv | 0.13 | 12 | ||
rs9257809 | 0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 | 10 | ||
rs2178146 | 0.827 | 0.080 | 16 | 86430089 | downstream gene variant | T/C | snv | 0.31 | 8 | ||
rs11789015 | 0.882 | 0.080 | 9 | 93953746 | intron variant | A/C;G | snv | 6 | |||
rs2687201 | 0.925 | 0.080 | 3 | 70879779 | intergenic variant | A/C;G | snv | 6 | |||
rs3784262 | 0.882 | 0.160 | 15 | 57960908 | intron variant | T/A;C | snv | 6 | |||
rs10419226 | 0.925 | 0.080 | 19 | 18692362 | intron variant | T/G | snv | 0.67 | 5 | ||
rs4800353 | 0.925 | 0.080 | 18 | 22074176 | intergenic variant | A/G | snv | 0.30 | 5 | ||
rs7632500 | 0.925 | 0.080 | 3 | 168007561 | downstream gene variant | A/G | snv | 0.17 | 5 | ||
rs11901649 | 0.882 | 0.080 | 2 | 21027351 | intron variant | G/A;C;T | snv | 3 | |||
rs4676893 | 0.882 | 0.080 | 3 | 70868488 | intergenic variant | A/T | snv | 0.61 | 3 | ||
rs7255 | 0.925 | 0.080 | 2 | 20679060 | 3 prime UTR variant | T/A;C | snv | 3 | |||
rs10108511 | 0.925 | 0.080 | 8 | 11578007 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs1247942 | 0.925 | 0.080 | 12 | 114235918 | downstream gene variant | G/A;C | snv | 2 | |||
rs1263178238 | 0.925 | 0.080 | 19 | 51338047 | missense variant | T/C | snv | 2.6E-05 | 4.9E-05 | 2 | |
rs17451754 | 0.925 | 0.080 | 7 | 117616658 | intron variant | G/A | snv | 0.10 | 2 | ||
rs17749155 | 0.925 | 0.080 | 8 | 10210563 | intron variant | G/A | snv | 0.16 | 2 | ||
rs1979654 | 0.925 | 0.080 | 16 | 86363229 | TF binding site variant | G/C | snv | 0.55 | 2 | ||
rs199620551 | 0.925 | 0.080 | 19 | 18693485 | intron variant | G/- | del | 9.2E-02 | 2 | ||
rs2464469 | 0.925 | 0.080 | 15 | 58069827 | intron variant | G/A | snv | 0.65 | 2 |