Source: INFERRED ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 4 | ||||
| rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
| rs10864728 | 1 | 230169168 | intron variant | A/G | snv | 0.50 | 3 | ||||
| rs10900522 | 1 | 205714939 | 3 prime UTR variant | T/C | snv | 0.21 | 4 | ||||
| rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
| rs11571111 | 1 | 204161105 | intron variant | C/A | snv | 5.0E-03 | 4 | ||||
| rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 8 | ||
| rs1321257 | 1 | 230169566 | intron variant | G/A | snv | 0.50 | 2 | ||||
| rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
| rs17315646 | 1 | 230159560 | intron variant | C/A;G | snv | 0.45 | 4 | ||||
| rs193084249 | 1 | 26661155 | intergenic variant | A/G | snv | 1.7E-02 | 3 | ||||
| rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 4 | ||
| rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs2296065 | 1 | 230166030 | intron variant | G/A;C | snv | 3 | |||||
| rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
| rs2785990 | 1 | 219514090 | intergenic variant | C/T | snv | 0.73 | 2 | ||||
| rs2791547 | 1 | 219486326 | intergenic variant | A/T | snv | 0.51 | 2 | ||||
| rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
| rs3753600 | 1 | 53125615 | intron variant | G/A | snv | 3.0E-03 | 3 | ||||
| rs4495740 | 1 | 62658794 | intron variant | T/G | snv | 0.34 | 5 | ||||
| rs480392 | 1 | 107436774 | synonymous variant | A/C | snv | 0.99 | 0.95 | 3 | |||
| rs4846914 | 0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 | 4 | ||
| rs4846918 | 1 | 230164840 | intron variant | C/G;T | snv | 3 | |||||
| rs4846923 | 1 | 230171476 | intron variant | T/G | snv | 0.72 | 2 | ||||
| rs4847240 | 1 | 93352389 | intron variant | A/G | snv | 0.51 | 3 |