Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893768 | 0.807 | 0.080 | 3 | 129528801 | missense variant | C/A | snv | 11 | |||
rs29001566 | 0.807 | 0.080 | 3 | 129533711 | missense variant | C/A;G;T | snv | 10 | |||
rs104894673 | 0.776 | 0.160 | 19 | 47839335 | missense variant | C/T | snv | 2.1E-05 | 8 | ||
rs121434631 | 0.807 | 0.080 | 6 | 42179248 | missense variant | C/G;T | snv | 4.0E-06 | 6 | ||
rs61752871 | 0.827 | 0.080 | 1 | 68444858 | missense variant | G/A | snv | 5.6E-05 | 6.3E-05 | 6 | |
rs1177783734 | 0.925 | 0.080 | 8 | 18083991 | missense variant | T/G | snv | 4.5E-06 | 7.0E-06 | 4 | |
rs104893779 | 0.851 | 0.080 | 3 | 129532288 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs527236100 | 0.851 | 0.080 | 3 | 129532282 | missense variant | G/A | snv | 4 | |||
rs397514601 | 0.882 | 0.040 | 11 | 77115423 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
rs281865362 | 0.882 | 0.040 | X | 18642053 | missense variant | C/T | snv | 3 | |||
rs267607034 | 0.882 | 0.080 | 1 | 156163009 | missense variant | T/G | snv | 3 | |||
rs61752159 | 0.925 | 0.040 | X | 18644530 | missense variant | C/T | snv | 2 | |||
rs121909835 | 0.925 | 0.040 | 5 | 149883511 | missense variant | C/T | snv | 5.2E-05 | 6.3E-05 | 2 | |
rs759589388 | 0.925 | 0.080 | 5 | 149895227 | missense variant | G/A | snv | 1.2E-05 | 2 | ||
rs1409112179 | 1.000 | 0.040 | 8 | 54621163 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs746231050 | 1.000 | 0.040 | 22 | 40404615 | missense variant | G/A | snv | 1.2E-05 | 3.5E-05 | 1 |