Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913450 | 1.000 | 0.080 | 9 | 130873016 | missense variant | A/G | snv | 1 | |||
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 | |||
rs121913453 | 1.000 | 0.080 | 9 | 130862962 | missense variant | G/A | snv | 1 | |||
rs121913454 | 0.925 | 0.080 | 9 | 130874969 | missense variant | A/G | snv | 2 | |||
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 | |||
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs121913460 | 0.925 | 0.080 | 9 | 130862971 | missense variant | A/T | snv | 2 | |||
rs121913461 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 5 | |||
rs121913505 | 0.925 | 0.080 | 4 | 54695598 | missense variant | G/A | snv | 2.0E-05 | 2 | ||
rs121913507 | 0.614 | 0.400 | 4 | 54733155 | missense variant | A/T | snv | 49 | |||
rs121913516 | 1.000 | 0.080 | 4 | 54729353 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs121913615 | 0.683 | 0.240 | 1 | 43349338 | missense variant | G/C;T | snv | 8.0E-06 | 25 | ||
rs121913682 | 0.605 | 0.400 | 4 | 54733167 | missense variant | A/G;T | snv | 52 | |||
rs12343867 | 0.790 | 0.200 | 9 | 5074189 | intron variant | T/C | snv | 0.25 | 9 | ||
rs1239681664 | 0.716 | 0.320 | 9 | 104818690 | synonymous variant | A/G | snv | 7.0E-06 | 15 | ||
rs1250394819 | 0.807 | 0.240 | 5 | 115616325 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs1257378 | 1.000 | 0.080 | 11 | 94621792 | intron variant | A/T | snv | 1 | |||
rs12573787 | 1.000 | 0.080 | 10 | 87863959 | 5 prime UTR variant | G/A;C | snv | 1 | |||
rs1314838108 | 0.925 | 0.160 | 9 | 130854977 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1343187782 | 1.000 | 0.080 | 3 | 37298923 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs1353702185 | 0.550 | 0.720 | 12 | 68839311 | missense variant | C/G | snv | 4.0E-06 | 79 |