Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3801004 | 0.882 | 0.120 | 7 | 5598591 | intron variant | C/A;G;T | snv | 3 | |||
rs560890523 | 1.000 | 0.080 | 12 | 25205729 | 3 prime UTR variant | TT/-;T | delins | 3 | |||
rs17530068 | 0.882 | 0.120 | 6 | 81483392 | intergenic variant | T/C | snv | 0.19 | 3 | ||
rs3760468 | 0.882 | 0.120 | 17 | 51153130 | upstream gene variant | A/T | snv | 0.39 | 3 | ||
rs2253319 | 0.882 | 0.120 | 21 | 34815749 | intron variant | C/G;T | snv | 3 | |||
rs6762208 | 0.851 | 0.200 | 3 | 185613377 | missense variant | C/A;T | snv | 0.36; 1.2E-05 | 3 | ||
rs184432 | 0.882 | 0.120 | 21 | 42367453 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
rs225359 | 0.882 | 0.120 | 21 | 42367327 | upstream gene variant | G/A | snv | 0.62 | 3 | ||
rs6990097 | 0.882 | 0.120 | 8 | 9555347 | non coding transcript exon variant | T/C | snv | 0.28 | 3 | ||
rs10754339 | 0.882 | 0.120 | 1 | 117147650 | 3 prime UTR variant | G/A | snv | 0.88 | 0.76 | 3 | |
rs8176746 | 0.882 | 0.160 | 9 | 133255935 | missense variant | G/A;T | snv | 4.1E-06; 0.12 | 4 | ||
rs12774070 | 0.925 | 0.120 | 10 | 70753879 | missense variant | C/A;G | snv | 0.23 | 0.19 | 4 | |
rs2071676 | 0.925 | 0.120 | 9 | 35674056 | missense variant | G/A | snv | 0.37 | 0.30 | 4 | |
rs2064863 | 0.925 | 0.120 | 20 | 56387716 | intron variant | T/A;C;G | snv | 4 | |||
rs3748093 | 0.925 | 0.120 | 7 | 140800651 | intron variant | T/A | snv | 1.5E-02 | 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 | ||
rs738722 | 0.882 | 0.120 | 22 | 28734024 | intron variant | T/C | snv | 0.67 | 4 | ||
rs6720283 | 0.882 | 0.120 | 2 | 237401239 | intron variant | G/A | snv | 0.31 | 4 | ||
rs77382849 | 0.851 | 0.160 | 10 | 119050586 | missense variant | C/T | snv | 8.8E-03 | 4.4E-03 | 4 | |
rs9679162 | 0.882 | 0.120 | 2 | 31024648 | intron variant | G/T | snv | 0.48 | 4 | ||
rs2105269 | 0.882 | 0.120 | 14 | 69280517 | intron variant | A/G | snv | 0.35 | 4 | ||
rs3917356 | 0.882 | 0.160 | 2 | 112834786 | intron variant | C/T | snv | 0.39 | 4 | ||
rs1799817 | 0.851 | 0.200 | 19 | 7125286 | synonymous variant | G/A | snv | 0.23 | 0.21 | 4 | |
rs4719839 | 0.882 | 0.120 | 7 | 25946953 | downstream gene variant | G/A;C | snv | 4 |