Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs980303898 | 0.851 | 0.120 | 2 | 162147479 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 4 | |
rs2762932 | 0.882 | 0.200 | 20 | 54151852 | downstream gene variant | T/C | snv | 0.17 | 3 | ||
rs10887710 | 0.925 | 0.120 | 10 | 80270029 | downstream gene variant | T/C | snv | 0.19 | 2 | ||
rs11644043 | 0.925 | 0.120 | 16 | 50327466 | intron variant | T/C | snv | 0.24 | 2 | ||
rs12362504 | 0.925 | 0.120 | 11 | 9907995 | intron variant | T/C | snv | 0.37 | 2 | ||
rs1276300653 | 0.925 | 0.120 | 3 | 9757072 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs1339638227 | 0.925 | 0.120 | 9 | 21971119 | missense variant | T/C | snv | 4.3E-06 | 2 | ||
rs1448106115 | 0.925 | 0.120 | 7 | 5989944 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs145574072 | 0.925 | 0.120 | 3 | 9754765 | synonymous variant | T/C | snv | 4.0E-06 | 2 | ||
rs17458086 | 0.925 | 0.120 | 12 | 40034837 | intron variant | T/C | snv | 1.1E-02 | 2 | ||
rs2074733 | 0.925 | 0.120 | 22 | 30342598 | non coding transcript exon variant | T/C | snv | 0.53 | 2 | ||
rs2457571 | 0.925 | 0.120 | 6 | 160413796 | intron variant | T/C | snv | 0.62 | 2 | ||
rs3124761 | 0.925 | 0.120 | 9 | 133474633 | intron variant | T/C | snv | 0.80 | 2 | ||
rs4927850 | 0.925 | 0.120 | 3 | 196024759 | intron variant | T/C | snv | 0.71 | 2 | ||
rs767964519 | 0.925 | 0.120 | 2 | 177231869 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs782095550 | 0.925 | 0.120 | 3 | 51386267 | missense variant | T/C | snv | 2 | |||
rs7106914 | 1.000 | 0.120 | 11 | 9956424 | intron variant | T/C | snv | 0.38 | 1 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs200349340 | 0.925 | 0.120 | 12 | 53962704 | non coding transcript exon variant | T/A;G | snv | 2 | |||
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs2066827 | 0.695 | 0.320 | 12 | 12718165 | missense variant | T/A;C;G | snv | 1.6E-04; 1.6E-05; 0.26 | 21 | ||
rs1447826 | 1.000 | 0.120 | 3 | 74669607 | intergenic variant | T/A;C;G | snv | 1 | |||
rs5219 | 0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 | 25 | ||
rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
rs1799966 | 0.807 | 0.280 | 17 | 43071077 | missense variant | T/A;C | snv | 5.2E-05; 0.35 | 8 |