Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12666409 | 1.000 | 0.080 | 7 | 50567279 | upstream gene variant | T/A | snv | 0.21 | 1 | ||
rs74501188 | 1.000 | 0.080 | 5 | 90931162 | 5 prime UTR variant | G/A | snv | 0.17 | 1 | ||
rs717620 | 0.763 | 0.240 | 10 | 99782821 | 5 prime UTR variant | C/T | snv | 0.17 | 0.15 | 10 | |
rs3124599 | 0.851 | 0.080 | 9 | 136509318 | intron variant | G/A | snv | 0.13 | 5 | ||
rs4760 | 1.000 | 0.080 | 19 | 43648948 | missense variant | A/G | snv | 0.12 | 0.11 | 8 | |
rs1045494 | 0.882 | 0.120 | 2 | 201287058 | 3 prime UTR variant | T/C | snv | 0.10 | 3 | ||
rs12200782 | 1.000 | 0.080 | 6 | 26402808 | intron variant | C/G | snv | 7.9E-02 | 1 | ||
rs141670911 | 1.000 | 0.080 | 6 | 26581030 | intergenic variant | A/T | snv | 7.3E-02 | 1 | ||
rs4324798 | 0.790 | 0.240 | 6 | 28808340 | intergenic variant | G/A | snv | 7.2E-02 | 8 | ||
rs17185553 | 1.000 | 0.080 | 9 | 17934122 | intron variant | G/C | snv | 6.5E-02 | 1 | ||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs1138272 | 0.611 | 0.600 | 11 | 67586108 | missense variant | C/T | snv | 5.9E-02 | 5.5E-02 | 42 | |
rs4866 | 0.827 | 0.240 | 7 | 2249951 | missense variant | G/A | snv | 2.2E-02 | 1.8E-02 | 5 | |
rs140013431 | 1.000 | 0.080 | 6 | 7770278 | intron variant | T/C | snv | 1.2E-02 | 1 | ||
rs56391007 | 0.752 | 0.200 | 7 | 116771936 | missense variant | C/T | snv | 7.9E-03 | 9.0E-03 | 16 | |
rs141877527 | 1.000 | 0.080 | 10 | 33497992 | intergenic variant | A/G | snv | 7.3E-03 | 1 | ||
rs117729306 | 1.000 | 0.080 | 11 | 8465623 | non coding transcript exon variant | T/C | snv | 7.3E-03 | 1 | ||
rs11571833 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 43 | |
rs34589476 | 0.827 | 0.160 | 7 | 116771869 | missense variant | C/T | snv | 2.9E-03 | 3.2E-03 | 7 | |
rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
rs1429133479 | 1.000 | 0.080 | 22 | 25847461 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
rs148924904 | 0.724 | 0.360 | 17 | 7675124 | missense variant | T/C | snv | 7.0E-06 | 17 | ||
rs577715207 | 0.827 | 0.160 | 3 | 189886413 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 8 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 |