Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs796065343 | 0.776 | 0.080 | 1 | 36467833 | missense variant | G/A | snv | 12 | |||
rs121913516 | 1.000 | 0.080 | 4 | 54729353 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs1360131632 | 0.827 | 0.080 | 17 | 42301316 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs121913452 | 0.851 | 0.080 | 9 | 130873027 | missense variant | T/A;C;G | snv | 4 | |||
rs1057519771 | 1.000 | 0.080 | 9 | 130872201 | missense variant | G/C | snv | 2 | |||
rs111340708 | 0.925 | 0.080 | 12 | 111447548 | intron variant | TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG | delins | 0.52 | 2 | ||
rs121913454 | 0.925 | 0.080 | 9 | 130874969 | missense variant | A/G | snv | 2 | |||
rs121913460 | 0.925 | 0.080 | 9 | 130862971 | missense variant | A/T | snv | 2 | |||
rs121913505 | 0.925 | 0.080 | 4 | 54695598 | missense variant | G/A | snv | 2.0E-05 | 2 | ||
rs918140013 | 0.925 | 0.080 | 12 | 111447663 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1057519758 | 1.000 | 0.080 | 9 | 130872153 | missense variant | T/G | snv | 1 | |||
rs1057519772 | 1.000 | 0.080 | 9 | 130872895 | missense variant | A/G | snv | 1 | |||
rs1057519774 | 1.000 | 0.080 | 9 | 130872902 | missense variant | T/G | snv | 1 | |||
rs1057519775 | 1.000 | 0.080 | 9 | 130873028 | missense variant | T/G | snv | 1 | |||
rs1057519776 | 1.000 | 0.080 | 1 | 36467843 | missense variant | T/C | snv | 1 | |||
rs1064156 | 1.000 | 0.080 | 9 | 130878519 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1178702025 | 1.000 | 0.080 | 18 | 44951912 | missense variant | G/A | snv | 1 | |||
rs121913449 | 1.000 | 0.080 | 9 | 130862977 | missense variant | A/T | snv | 1 | |||
rs121913450 | 1.000 | 0.080 | 9 | 130873016 | missense variant | A/G | snv | 1 | |||
rs121913453 | 1.000 | 0.080 | 9 | 130862962 | missense variant | G/A | snv | 1 | |||
rs121913455 | 1.000 | 0.080 | 9 | 130862955 | missense variant | C/G | snv | 1 | |||
rs121913456 | 1.000 | 0.080 | 9 | 130862943 | missense variant | A/G | snv | 1 | |||
rs121913457 | 1.000 | 0.080 | 9 | 130873004 | missense variant | T/C | snv | 1 | |||
rs121913458 | 1.000 | 0.080 | 9 | 130862969 | missense variant | G/C;T | snv | 1 | |||
rs1257378 | 1.000 | 0.080 | 11 | 94621792 | intron variant | A/T | snv | 1 |