Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs387906517 | 0.827 | 0.120 | 9 | 130862919 | missense variant | G/A | snv | 6 | |||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs121913461 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 5 | |||
rs1057519773 | 0.851 | 0.160 | 9 | 130872901 | missense variant | T/A;C;G | snv | 4 | |||
rs121913451 | 0.851 | 0.160 | 9 | 130872903 | missense variant | C/A;G | snv | 4 | |||
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 | |||
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 | |||
rs1314838108 | 0.925 | 0.160 | 9 | 130854977 | 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 | |||
rs1064156 | 1.000 | 0.080 | 9 | 130878519 | missense variant | G/A | snv | 4.0E-06 | 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 | |||
rs34549764 | 1.000 | 0.080 | 9 | 130862953 | missense variant | A/G | snv | 2.6E-03 | 2.5E-03 | 1 |