Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3761548 | 0.620 | 0.680 | X | 49261784 | intron variant | G/A;T | snv | 42 | |||
rs1057519912 | 0.776 | 0.200 | X | 71129408 | missense variant | C/G;T | snv | 11 | |||
rs137852569 | 0.752 | 0.320 | X | 67686030 | missense variant | G/A | snv | 9.4E-06 | 10 | ||
rs137852578 | 0.827 | 0.080 | X | 67723710 | missense variant | A/G | snv | 10 | |||
rs6152 | 0.763 | 0.240 | X | 67545785 | synonymous variant | G/A | snv | 0.15 | 0.28 | 9 | |
rs1057519864 | 0.851 | 0.080 | X | 67723707 | missense variant | T/C | snv | 8 | |||
rs137852593 | 0.827 | 0.160 | X | 67717484 | missense variant | G/A;C;T | snv | 2.2E-05; 1.1E-05; 9.1E-04 | 8 | ||
rs976306779 | 0.851 | 0.080 | X | 67545492 | missense variant | C/A;T | snv | 6.6E-06 | 8 | ||
rs137852564 | 0.827 | 0.240 | X | 67722976 | missense variant | G/A;T | snv | 5 | |||
rs137852581 | 0.882 | 0.080 | X | 67723701 | missense variant | C/T | snv | 5 | |||
rs864622007 | 0.882 | 0.200 | X | 67711621 | missense variant | T/A | snv | 5 | |||
rs1034866440 | 0.851 | 0.160 | X | 67643401 | missense variant | G/A | snv | 5.7E-06 | 4 | ||
rs137852591 | 0.851 | 0.200 | X | 67721909 | missense variant | C/G | snv | 1.4E-03 | 1.4E-03 | 4 | |
rs1327301 | 0.882 | 0.160 | X | 51467205 | downstream gene variant | C/T | snv | 0.29 | 3 | ||
rs1340026226 | 1.000 | 0.080 | X | 67711662 | missense variant | G/A | snv | 9.5E-06 | 3 | ||
rs137852567 | 0.882 | 0.200 | X | 67717595 | missense variant | A/G | snv | 3 | |||
rs137852571 | 0.882 | 0.080 | X | 67717495 | missense variant | G/A | snv | 7.7E-05 | 1.9E-05 | 3 | |
rs5919432 | 0.882 | 0.160 | X | 67801708 | intergenic variant | C/T | snv | 3 | |||
rs5945572 | 0.882 | 0.160 | X | 51486831 | downstream gene variant | A/G | snv | 3 | |||
rs5945619 | 0.882 | 0.160 | X | 51498820 | non coding transcript exon variant | C/T | snv | 3 | |||
rs6624304 | 0.882 | 0.160 | X | 67655914 | intron variant | T/A;C | snv | 3 | |||
rs968098233 | 0.882 | 0.200 | X | 67546162 | missense variant | T/C | snv | 3 | |||
rs137852580 | 0.925 | 0.080 | X | 67723711 | missense variant | C/G;T | snv | 2 | |||
rs137852582 | 0.925 | 0.080 | X | 67723786 | missense variant | A/G | snv | 2 | |||
rs137852583 | 0.925 | 0.080 | X | 67711680 | missense variant | G/A | snv | 2 |