Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894584 | 0.851 | 0.120 | 17 | 70175553 | missense variant | G/A | snv | 5 | |||
rs1057518920 | 0.925 | 0.080 | 6 | 7575386 | stop gained | C/A | snv | 5 | |||
rs1554093433 | 0.925 | 0.080 | 5 | 173232833 | stop gained | G/T | snv | 4 | |||
rs190140598 | 0.851 | 0.120 | 1 | 237445488 | missense variant | C/A;T | snv | 1.2E-05 | 4 | ||
rs199472708 | 0.882 | 0.080 | 11 | 2572015 | missense variant | G/A | snv | 4 | |||
rs199473229 | 0.882 | 0.120 | 3 | 38560361 | missense variant | A/G | snv | 4 | |||
rs397514616 | 0.851 | 0.120 | 3 | 52452217 | missense variant | C/A;T | snv | 4 | |||
rs121912516 | 0.882 | 0.120 | 7 | 150951721 | missense variant | C/G | snv | 3 | |||
rs9388451 | 0.882 | 0.120 | 6 | 125769231 | regulatory region variant | T/A;C | snv | 3 | |||
rs199473574 | 0.925 | 0.120 | 3 | 38603951 | missense variant | C/T | snv | 2 | |||
rs188043534 | 1.000 | 0.080 | 12 | 38316992 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
rs192749597 | 0.882 | 0.080 | 12 | 2679712 | missense variant | C/T | snv | 9.2E-04 | 3.5E-03 | 3 | |
rs6125 | 0.925 | 0.080 | 1 | 169613079 | missense variant | C/T | snv | 5.6E-02 | 5.2E-02 | 2 | |
rs12090554 | 0.925 | 0.080 | 1 | 185583216 | intron variant | G/A | snv | 0.15 | 2 | ||
rs11720524 | 0.882 | 0.080 | 3 | 38633921 | intron variant | C/G;T | snv | 0.34 | 3 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs2824292 | 0.925 | 0.080 | 21 | 17414857 | regulatory region variant | G/A | snv | 0.47 | 3 | ||
rs6795970 | 0.807 | 0.200 | 3 | 38725184 | missense variant | A/G | snv | 0.65 | 0.70 | 13 | |
rs1353342 | 0.925 | 0.080 | 9 | 76259853 | intron variant | A/C | snv | 0.79 | 2 |