Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1340827343 | 0.851 | 0.040 | 6 | 31165259 | missense variant | C/T | snv | 4 | |||
rs1381537616 | 0.851 | 0.040 | 7 | 27174132 | missense variant | C/T | snv | 4 | |||
rs1415342243 | 0.851 | 0.040 | 6 | 26225549 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs144551722 | 0.851 | 0.040 | X | 43632629 | intergenic variant | G/A | snv | 0.13 | 4 | ||
rs1801591 | 0.882 | 0.040 | 15 | 76286421 | missense variant | G/A | snv | 7.4E-02 | 6.4E-02 | 4 | |
rs1957106 | 0.851 | 0.040 | 14 | 35404564 | synonymous variant | G/A | snv | 0.28 | 0.25 | 4 | |
rs200187877 | 0.851 | 0.040 | 4 | 23795829 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 4 | |
rs2017309 | 0.851 | 0.040 | 22 | 28735438 | intron variant | T/A | snv | 0.23 | 4 | ||
rs2235573 | 0.882 | 0.040 | 22 | 38081923 | synonymous variant | G/A | snv | 0.47 | 0.46 | 4 | |
rs2562152 | 0.882 | 0.040 | 16 | 73898 | intron variant | A/T | snv | 0.67 | 4 | ||
rs28357681 | 0.851 | 0.040 | MT | 14798 | missense variant | T/C | snv | 4 | |||
rs375391381 | 0.851 | 0.040 | 15 | 43883735 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 4 | |
rs3851634 | 0.882 | 0.040 | 12 | 106419124 | intron variant | T/C | snv | 0.22 | 4 | ||
rs572480837 | 0.851 | 0.040 | 6 | 31165582 | missense variant | T/A | snv | 5.0E-04 | 8.4E-05 | 4 | |
rs59060240 | 0.882 | 0.040 | 7 | 55080369 | intron variant | AA/-;A;AAA;AAAA;AAAAAAAAAAA | delins | 4 | |||
rs6062302 | 0.882 | 0.040 | 20 | 63689615 | synonymous variant | T/C | snv | 0.74 | 0.81 | 4 | |
rs648044 | 0.882 | 0.040 | 11 | 114160077 | non coding transcript exon variant | A/G;T | snv | 4 | |||
rs723527 | 0.882 | 0.040 | 7 | 55067179 | intron variant | A/G | snv | 0.53 | 4 | ||
rs75061358 | 0.882 | 0.040 | 7 | 54848587 | intergenic variant | T/C;G | snv | 4 | |||
rs755794544 | 0.851 | 0.040 | 7 | 512435 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
rs757066045 | 0.882 | 0.040 | 9 | 21974725 | missense variant | C/T | snv | 8.2E-06 | 4 | ||
rs760090729 | 0.851 | 0.040 | 6 | 27810468 | missense variant | G/A | snv | 4 | |||
rs766265850 | 0.851 | 0.040 | 6 | 30889239 | missense variant | G/A | snv | 8.1E-06 | 7.0E-06 | 4 | |
rs8057643 | 0.851 | 0.040 | 16 | 6910689 | intron variant | C/A;T | snv | 4 | |||
rs863225401 | 0.925 | 0.040 | 2 | 47799866 | stop gained | G/A | snv | 4 |