Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2001389 | 0.925 | 0.120 | 10 | 102615501 | intron variant | G/A;C | snv | 3 | |||
rs2027605 | 1.000 | 0.120 | 21 | 29354452 | intron variant | A/G | snv | 0.48 | 3 | ||
rs2235108 | 0.925 | 0.120 | 8 | 125436547 | 3 prime UTR variant | G/A | snv | 0.25 | 3 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 3 | ||
rs397507851 | 0.925 | 0.120 | 13 | 32340761 | frameshift variant | AAATGTT/- | delins | 3 | |||
rs4269383 | 0.882 | 0.120 | 6 | 155876368 | intergenic variant | A/G | snv | 0.37 | 3 | ||
rs757748401 | 0.925 | 0.120 | 20 | 51542465 | missense variant | C/A;T | snv | 5.2E-06 | 3 | ||
rs876659900 | 0.925 | 0.120 | 7 | 5982861 | stop gained | G/A | snv | 3 | |||
rs1034925236 | 0.925 | 0.120 | 1 | 200048258 | missense variant | G/C | snv | 2 | |||
rs10500715 | 0.925 | 0.120 | 11 | 9951515 | intron variant | T/G | snv | 0.39 | 2 | ||
rs10887710 | 0.925 | 0.120 | 10 | 80270029 | downstream gene variant | T/C | snv | 0.19 | 2 | ||
rs11085754 | 0.925 | 0.120 | 19 | 11017920 | intron variant | A/G | snv | 0.41 | 2 | ||
rs1153280 | 1.000 | 0.120 | 21 | 29305751 | intron variant | G/A | snv | 0.52 | 2 | ||
rs11644043 | 0.925 | 0.120 | 16 | 50327466 | intron variant | T/C | snv | 0.24 | 2 | ||
rs1235228469 | 0.925 | 0.120 | 3 | 138684714 | missense variant | C/A | snv | 8.0E-06 | 2 | ||
rs12362504 | 0.925 | 0.120 | 11 | 9907995 | intron variant | T/C | snv | 0.37 | 2 | ||
rs12456874 | 0.925 | 0.120 | 18 | 13366863 | intron variant | A/G | snv | 0.20 | 2 | ||
rs1276300653 | 0.925 | 0.120 | 3 | 9757072 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs12939944 | 0.925 | 0.120 | 17 | 12056502 | intron variant | C/T | snv | 0.45 | 2 | ||
rs1318 | 0.925 | 0.120 | 17 | 67695266 | 3 prime UTR variant | A/G | snv | 0.30 | 2 | ||
rs13303010 | 0.925 | 0.120 | 1 | 959193 | intron variant | G/A | snv | 0.82 | 0.69 | 2 | |
rs1336539869 | 0.925 | 0.120 | 12 | 57751681 | missense variant | C/G | snv | 2 | |||
rs1339638227 | 0.925 | 0.120 | 9 | 21971119 | missense variant | T/C | snv | 4.3E-06 | 2 | ||
rs138147246 | 0.925 | 0.120 | 3 | 9756551 | synonymous variant | A/G | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs139632793 | 0.925 | 0.120 | 3 | 9751114 | missense variant | G/C | snv | 5.2E-05 | 1.7E-04 | 2 |