Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10833 | 0.776 | 0.160 | 4 | 141733394 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs4074 | 0.827 | 0.200 | 4 | 73870427 | intron variant | A/G | snv | 0.46 | 6 | ||
rs5743314 | 0.851 | 0.160 | 4 | 186079221 | intron variant | G/C;T | snv | 5 | |||
rs10433937 | 0.882 | 0.080 | 4 | 87308948 | intron variant | T/A;C;G | snv | 4 | |||
rs1879026 | 1.000 | 0.080 | 4 | 186079167 | intron variant | G/C;T | snv | 3 | |||
rs111200466 | 1.000 | 0.080 | 4 | 153684312 | 5 prime UTR variant | CGGCTGCTCGGCGTTCTCTCAGG/- | delins | 0.17 | 2 | ||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs2243250 | 0.570 | 0.760 | 5 | 132673462 | upstream gene variant | C/T | snv | 0.35 | 61 | ||
rs6897932 | 0.683 | 0.560 | 5 | 35874473 | missense variant | C/T | snv | 0.23 | 0.21 | 25 | |
rs1281032650 | 5 | 96979168 | missense variant | A/G | snv | 1 | |||||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1800730 | 0.649 | 0.480 | 6 | 26090957 | missense variant | A/T | snv | 1.0E-02 | 1.0E-02 | 32 | |
rs2596542 | 0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 | 18 | ||
rs762623 | 1.000 | 0.160 | 6 | 36677689 | non coding transcript exon variant | G/A | snv | 0.12 | 2 | ||
rs1325863623 | 6 | 2953175 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs2071025 | 6 | 33175979 | intron variant | A/G | snv | 0.28 | 0.29 | 1 | |||
rs3116996 | 6 | 33130187 | downstream gene variant | T/A | snv | 0.13 | 1 | ||||
rs61750420 | 0.689 | 0.480 | 7 | 92501562 | missense variant | C/T | snv | 3.2E-04 | 3.5E-04 | 52 | |
rs75961395 | 0.763 | 0.280 | 7 | 117509123 | missense variant | G/A;T | snv | 4.0E-05 | 10 | ||
rs1051861187 | 0.827 | 0.080 | 7 | 87409385 | missense variant | A/G | snv | 6 | |||
rs751703423 | 7 | 6023410 | missense variant | G/A;C | snv | 1 | |||||
rs1420111973 | 1.000 | 0.080 | 9 | 117712527 | synonymous variant | T/C | snv | 7.0E-06 | 2 | ||
rs7096206 | 0.708 | 0.480 | 10 | 52771925 | upstream gene variant | G/A;C;T | snv | 17 | |||
rs1316569885 | 10 | 95399139 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |