Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434475 | 1.000 | 0.080 | MT | 9997 | non coding transcript exon variant | T/C | snv | 1 | |||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs199476321 | 0.882 | 0.080 | 15 | 63064133 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs199476317 | 0.827 | 0.080 | 15 | 63062263 | missense variant | G/A | snv | 6 | |||
rs199476316 | 0.925 | 0.080 | 15 | 63062219 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs199476315 | 0.827 | 0.080 | 15 | 63061723 | missense variant | G/A | snv | 5 | |||
rs104894502 | 0.807 | 0.120 | 15 | 63060915 | missense variant | A/G;T | snv | 6 | |||
rs104894503 | 0.776 | 0.160 | 15 | 63060899 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 9 | |
rs397516373 | 0.925 | 0.080 | 15 | 63059663 | missense variant | G/A | snv | 4 | |||
rs1555408679 | 1.000 | 0.080 | 15 | 63059648 | missense variant | A/G | snv | 1 | |||
rs1415568768 | 1.000 | 0.080 | 11 | 61965454 | missense variant | T/C | snv | 4.1E-06 | 1 | ||
rs727503506 | 1.000 | 0.080 | 19 | 55154743 | missense variant | C/G | snv | 8.0E-06 | 1 | ||
rs1568858210 | 1.000 | 0.080 | 19 | 55154175 | missense variant | A/G | snv | 1 | |||
rs730881069 | 1.000 | 0.080 | 19 | 55154172 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs397516347 | 0.851 | 0.120 | 19 | 55154157 | missense variant | C/T | snv | 4.2E-05 | 5 | ||
rs104894724 | 0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 | 8 | ||
rs397516349 | 0.807 | 0.080 | 19 | 55154145 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
rs397516353 | 0.882 | 0.080 | 19 | 55154109 | missense variant | G/A | snv | 3 | |||
rs368861241 | 0.851 | 0.120 | 19 | 55154095 | missense variant | G/A | snv | 4.0E-05 | 7.0E-06 | 4 | |
rs397516354 | 0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 | 8 | ||
rs727504242 | 0.925 | 0.080 | 19 | 55154082 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs727503504 | 0.807 | 0.080 | 19 | 55154071 | missense variant | G/A;C | snv | 6 | |||
rs727503503 | 0.827 | 0.120 | 19 | 55154070 | missense variant | C/T | snv | 5 | |||
rs727503501 | 1.000 | 0.080 | 19 | 55154053 | missense variant | C/T | snv | 1 | |||
rs397516351 | 0.925 | 0.080 | 19 | 55154045 | inframe deletion | TTC/- | delins | 2 |