Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35755165 | 0.882 | 0.080 | 19 | 40840084 | intron variant | A/C;G | snv | 5 | |||
rs36600 | 0.827 | 0.080 | 22 | 29941597 | intron variant | T/C | snv | 0.78 | 5 | ||
rs374733251 | 0.882 | 0.080 | 7 | 116740993 | missense variant | A/G | snv | 6.0E-05 | 7.7E-05 | 5 | |
rs377444977 | 0.882 | 0.080 | 7 | 55143443 | missense variant | G/A | snv | 5.2E-05 | 2.1E-05 | 5 | |
rs3842 | 0.882 | 0.080 | 7 | 87504050 | 3 prime UTR variant | T/C | snv | 0.16 | 5 | ||
rs4488809 | 0.827 | 0.080 | 3 | 189638472 | intron variant | T/C | snv | 0.45 | 5 | ||
rs4647958 | 0.851 | 0.080 | 20 | 49984094 | missense variant | T/C | snv | 0.18 | 0.29 | 5 | |
rs533748068 | 0.851 | 0.080 | 1 | 155950962 | missense variant | C/A;T | snv | 4.3E-06 | 7.0E-06 | 5 | |
rs5742933 | 0.882 | 0.080 | 2 | 189784590 | 5 prime UTR variant | G/A;C | snv | 5 | |||
rs5744724 | 0.882 | 0.080 | 5 | 75599649 | 3 prime UTR variant | G/C | snv | 5.4E-02 | 5 | ||
rs6790167 | 0.827 | 0.080 | 3 | 189869485 | intron variant | A/G | snv | 0.53 | 5 | ||
rs760943842 | 0.851 | 0.080 | 1 | 23362976 | missense variant | G/A | snv | 4.0E-05 | 1.4E-05 | 5 | |
rs775057330 | 0.851 | 0.080 | 12 | 25149651 | missense variant | C/A;T | snv | 5 | |||
rs775514340 | 0.882 | 0.080 | 6 | 53041202 | missense variant | T/A;C | snv | 4.0E-06 | 5 | ||
rs7969931 | 0.851 | 0.080 | 12 | 25089661 | missense variant | C/A;G | snv | 1.6E-05; 0.75 | 5 | ||
rs1046175 | 0.851 | 0.080 | 10 | 133391446 | stop gained | C/A;G;T | snv | 1.2E-05; 0.88 | 4 | ||
rs104886026 | 0.851 | 0.080 | 7 | 55200333 | missense variant | G/A | snv | 4 | |||
rs10519717 | 0.851 | 0.080 | 4 | 144559188 | intron variant | T/C | snv | 0.21 | 4 | ||
rs1057519857 | 0.882 | 0.080 | 17 | 39724772 | missense variant | T/C | snv | 4 | |||
rs1060501327 | 0.851 | 0.080 | 1 | 45332251 | missense variant | A/G | snv | 4 | |||
rs11072768 | 0.882 | 0.080 | 15 | 78637136 | intron variant | T/C;G | snv | 4 | |||
rs112290073 | 0.882 | 0.080 | 5 | 1285917 | intron variant | G/A | snv | 7.8E-03 | 4 | ||
rs11540478 | 0.851 | 0.080 | 15 | 90085305 | synonymous variant | G/A;C | snv | 3.5E-02; 6.4E-06 | 4 | ||
rs1169300 | 0.882 | 0.080 | 12 | 120993422 | intron variant | G/A | snv | 0.27 | 4 | ||
rs1171287261 | 0.851 | 0.080 | 7 | 55191839 | missense variant | G/A | snv | 4 |