Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
rs573658040 | 0.790 | 0.200 | 19 | 44908705 | missense variant | C/G;T | snv | 6.3E-06 | 9 | ||
rs1275147925 | 1.000 | 0.080 | 19 | 44906613 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs1458301734 | 1.000 | 0.080 | 19 | 44908687 | missense variant | G/A;T | snv | 5.9E-06 | 1 | ||
rs868094551 | 1.000 | 0.080 | 19 | 44908768 | missense variant | C/A;T | snv | 1 |