Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10754339 | 0.882 | 0.120 | 1 | 117147650 | 3 prime UTR variant | G/A | snv | 0.88 | 0.76 | 3 | |
rs1256054 | 0.882 | 0.120 | 14 | 64249595 | synonymous variant | G/C | snv | 2.8E-03 | 9.6E-04 | 3 | |
rs1455751791 | 0.882 | 0.120 | 6 | 152011735 | synonymous variant | C/G | snv | 4.0E-06 | 3 | ||
rs17530068 | 0.882 | 0.120 | 6 | 81483392 | intergenic variant | T/C | snv | 0.19 | 3 | ||
rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 3 | ||
rs3760468 | 0.882 | 0.120 | 17 | 51153130 | upstream gene variant | A/T | snv | 0.39 | 3 | ||
rs3801004 | 0.882 | 0.120 | 7 | 5598591 | intron variant | C/A;G;T | snv | 3 | |||
rs6762208 | 0.851 | 0.200 | 3 | 185613377 | missense variant | C/A;T | snv | 0.36; 1.2E-05 | 3 | ||
rs6990097 | 0.882 | 0.120 | 8 | 9555347 | non coding transcript exon variant | T/C | snv | 0.28 | 3 | ||
rs2105269 | 0.882 | 0.120 | 14 | 69280517 | intron variant | A/G | snv | 0.35 | 4 | ||
rs3218038 | 0.882 | 0.120 | 19 | 29814988 | intron variant | G/T | snv | 9.1E-02 | 4 | ||
rs438034 | 0.882 | 0.120 | 1 | 214657274 | stop gained | A/G;T | snv | 0.61 | 4 | ||
rs2881766 | 0.882 | 0.120 | 6 | 151797984 | intron variant | T/G | snv | 0.35 | 5 | ||
rs4784227 | 0.807 | 0.160 | 16 | 52565276 | intron variant | C/T | snv | 0.20 | 6 | ||
rs6024836 | 0.851 | 0.160 | 20 | 56369012 | downstream gene variant | G/A | snv | 0.42 | 6 | ||
rs10053538 | 0.807 | 0.160 | 5 | 157110499 | intron variant | C/A;T | snv | 7 | |||
rs7963551 | 0.807 | 0.160 | 12 | 912349 | 3 prime UTR variant | T/G | snv | 0.13 | 7 | ||
rs746429 | 0.882 | 0.120 | 11 | 65649963 | synonymous variant | G/A | snv | 0.31 | 0.30 | 8 | |
rs11730582 | 0.807 | 0.240 | 4 | 87975269 | non coding transcript exon variant | T/C | snv | 0.37 | 10 | ||
rs3020449 | 0.807 | 0.200 | 14 | 64306674 | intron variant | A/G;T | snv | 10 | |||
rs3741219 | 0.776 | 0.280 | 11 | 1995389 | non coding transcript exon variant | A/G | snv | 0.42 | 10 | ||
rs11225395 | 0.776 | 0.360 | 11 | 102725749 | intron variant | A/C;G | snv | 11 | |||
rs13293512 | 0.763 | 0.360 | 9 | 94167461 | intron variant | T/C | snv | 0.24 | 11 | ||
rs16949649 | 0.776 | 0.200 | 17 | 51152947 | upstream gene variant | T/C | snv | 0.39 | 12 | ||
rs931127 | 0.790 | 0.160 | 11 | 65637829 | upstream gene variant | G/A | snv | 0.49 | 12 |