Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
| rs145482150 | 15 | 99993107 | missense variant | C/T | snv | 2.0E-04 | 2.0E-04 | 1 | |||
| rs149578709 | 15 | 100132203 | intron variant | A/G | snv | 9.0E-03 | 5.2E-03 | 1 | |||
| rs2573625 | 15 | 99972953 | 3 prime UTR variant | C/T | snv | 0.62 | 1 | ||||
| rs2581348 | 15 | 99973858 | 3 prime UTR variant | C/T | snv | 0.63 | 1 | ||||
| rs2727195 | 15 | 99972912 | 3 prime UTR variant | G/A | snv | 0.61 | 1 | ||||
| rs28411867 | 15 | 100314288 | intron variant | C/T | snv | 0.19 | 1 | ||||
| rs397807524 | 15 | 100052239 | intron variant | -/AA | ins | 7.0E-06 | 1 | ||||
| rs4369638 | 15 | 100254158 | synonymous variant | C/T | snv | 0.75 | 0.76 | 1 | |||
| rs4467054 | 15 | 100255167 | intron variant | G/A;T | snv | 1 | |||||
| rs4533267 | 15 | 100246066 | intron variant | A/G | snv | 0.63 | 1 | ||||
| rs4965593 | 15 | 100218180 | intron variant | C/G;T | snv | 1 | |||||
| rs4965598 | 15 | 100219409 | intron variant | C/A;T | snv | 1 | |||||
| rs4965612 | 15 | 100261237 | intron variant | A/G | snv | 0.72 | 1 | ||||
| rs76301628 | 15 | 100183232 | intron variant | G/T | snv | 3.4E-02 | 1 | ||||
| rs2573652 | 15 | 99974409 | missense variant | T/C;G | snv | 0.66; 4.0E-06 | 1 |