Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs150844304 | 15 | 43434427 | intron variant | A/C;G | snv | 4 | |||||
rs4660293 | 1 | 39562508 | non coding transcript exon variant | A/C;G | snv | 4 | |||||
rs2943646 | 2 | 226234818 | intergenic variant | A/C;G | snv | 3 | |||||
rs5471 | 0.882 | 0.160 | 16 | 72054562 | 5 prime UTR variant | A/C;G | snv | 7.9E-03 | 3 | ||
rs10489615 | 1 | 230169242 | intron variant | A/C;G | snv | 2 | |||||
rs11765979 | 7 | 130761118 | intergenic variant | A/C;G | snv | 2 | |||||
rs2322549 | 4 | 142395874 | intron variant | A/C;G | snv | 2 | |||||
rs4285028 | 1.000 | 0.080 | 3 | 121941817 | 3 prime UTR variant | A/C;G | snv | 2 | |||
rs7254723 | 1.000 | 0.080 | 19 | 44952664 | intron variant | A/C;G | snv | 2 | |||
rs7847628 | 9 | 120868947 | intron variant | A/C;G | snv | 2 | |||||
rs2058804 | 12 | 109471206 | missense variant | A/C;G | snv | 0.50 | 1 | ||||
rs255054 | 16 | 67983453 | upstream gene variant | A/C;G | snv | 1 | |||||
rs6822892 | 4 | 156813523 | intron variant | A/C;G | snv | 1 | |||||
rs2980875 | 8 | 125469505 | intron variant | A/C;G;T | snv | 4 | |||||
rs9863753 | 3 | 52495883 | intron variant | A/C;G;T | snv | 2 | |||||
rs10937241 | 3 | 186104985 | non coding transcript exon variant | A/C;G;T | snv | 1 | |||||
rs2652834 | 15 | 63104668 | intron variant | A/C;G;T | snv | 1 | |||||
rs180349 | 0.925 | 0.200 | 11 | 116741111 | intergenic variant | A/C;T | snv | 3 | |||
rs6657811 | 1 | 109264661 | intron variant | A/C;T | snv | 4.0E-06; 0.10 | 3 | ||||
rs10955992 | 8 | 120860224 | intergenic variant | A/C;T | snv | 2 | |||||
rs970548 | 10 | 45517829 | intron variant | A/C;T | snv | 2 | |||||
rs10743940 | 12 | 7498542 | intron variant | A/C;T | snv | 1 | |||||
rs1945391 | 11 | 122649583 | regulatory region variant | A/C;T | snv | 1 | |||||
rs486394 | 1.000 | 0.040 | 11 | 116655605 | intron variant | A/C;T | snv | 1 | |||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 |