Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs2228611 | 0.708 | 0.520 | 19 | 10156401 | synonymous variant | T/A;C | snv | 0.52 | 19 | ||
rs1554603293 | 0.752 | 0.320 | 8 | 60849154 | missense variant | G/A | snv | 17 | |||
rs16999593 | 0.742 | 0.240 | 19 | 10180505 | missense variant | T/C | snv | 2.4E-02 | 9.6E-03 | 14 | |
rs528302390 | 0.776 | 0.120 | 7 | 47831214 | splice donor variant | AC/- | delins | 3.7E-04 | 5.0E-04 | 9 | |
rs121434422 | 0.882 | 0.120 | 19 | 18869035 | stop gained | G/A;C;T | snv | 3 | |||
rs61743125 | 0.882 | 0.080 | 6 | 42925677 | missense variant | G/A | snv | 2.0E-02 | 1.9E-02 | 3 | |
rs772953044 | 0.925 | 0.120 | 1 | 6333503 | missense variant | T/C;G | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs1424438515 | 0.925 | 0.080 | 4 | 186274140 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
rs1324026337 | 0.925 | 0.120 | 20 | 38148038 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs752163489 | 0.925 | 0.120 | 22 | 37096044 | stop gained | C/A;T | snv | 1.8E-04 | 2 | ||
rs16999358 | 1.000 | 0.080 | 19 | 10162679 | synonymous variant | G/A | snv | 6.2E-03 | 2.4E-03 | 1 | |
rs2276598 | 1.000 | 0.080 | 2 | 25246633 | synonymous variant | C/T | snv | 0.19 | 0.21 | 1 | |
rs2276599 | 1.000 | 0.080 | 2 | 25247044 | splice region variant | C/T | snv | 0.71 | 0.69 | 1 |