Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 7 | |||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 7 | |||
rs4246215 | 0.677 | 0.320 | 11 | 61796827 | 3 prime UTR variant | G/C;T | snv | 6 | |||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 3 | ||
rs13300663 | 9 | 4814948 | intron variant | G/A;C | snv | 3 | |||||
rs6141 | 0.925 | 0.080 | 3 | 184372478 | 3 prime UTR variant | C/G;T | snv | 4.0E-06; 0.56 | 3 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 2 | |||||
rs1668871 | 1 | 205268009 | intron variant | T/C;G | snv | 2 | |||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 2 | ||||
rs8176747 | 9 | 133255928 | missense variant | C/A;G | snv | 4.1E-06; 0.12 | 2 | ||||
rs1034566 | 22 | 19996754 | intron variant | C/G;T | snv | 1 | |||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 1 | |||||
rs11628318 | 14 | 102573750 | regulatory region variant | T/A;C | snv | 1 | |||||
rs11757577 | 6 | 135070327 | intron variant | G/A;T | snv | 1 | |||||
rs13042885 | 20 | 1944061 | upstream gene variant | C/A;T | snv | 1 | |||||
rs17568628 | 5 | 76751114 | intergenic variant | T/C;G | snv | 1 | |||||
rs1977081 | 1.000 | 22 | 43934248 | intron variant | T/C;G | snv | 1 | ||||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 1 | ||
rs3792366 | 3 | 123121029 | intron variant | G/A;T | snv | 1 | |||||
rs457287 | 9 | 4834394 | intron variant | A/G;T | snv | 1 | |||||
rs6995402 | 8 | 143931393 | intron variant | T/C | snv | 1 | |||||
rs700585 | 5 | 88856300 | intron variant | C/A;T | snv | 1 | |||||
rs3819299 | 1.000 | 6 | 31354590 | non coding transcript exon variant | T/G | snv | 7.7E-02 | 2.3E-02 | 5 |