Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867114783 | 17 | 7675109 | missense variant | T/C | snv | 6 | |||||
rs1802710 | 14 | 100734308 | synonymous variant | T/A;C | snv | 0.63 | 3 | ||||
rs12289961 | 11 | 58292720 | non coding transcript exon variant | C/T | snv | 0.28 | 1 | ||||
rs2647045 | 6 | 32700323 | TF binding site variant | G/A | snv | 0.27 | 1 | ||||
rs273429 | 8 | 131467654 | intergenic variant | C/T | snv | 0.43 | 1 | ||||
rs4530903 | 6 | 32614112 | intergenic variant | C/T | snv | 0.10 | 1 | ||||
rs948562 | 11 | 58580292 | intron variant | A/G | snv | 0.15 | 1 | ||||
rs74790047 | 0.851 | 0.120 | 12 | 6601978 | missense variant | A/C;G | snv | 2.0E-05; 1.2E-04; 5.2E-03 | 1.7E-03 | 7 | |
rs1353428252 | 0.851 | 0.120 | 15 | 90088681 | missense variant | A/C | snv | 8.0E-06 | 5 | ||
rs10190751 | 0.882 | 0.120 | 2 | 201141373 | splice acceptor variant | G/A | snv | 0.18 | 0.26 | 4 | |
rs751837 | 0.882 | 0.120 | 14 | 103018488 | intron variant | T/C | snv | 0.23 | 4 | ||
rs1042752 | 0.925 | 0.120 | 11 | 111352386 | 3 prime UTR variant | A/G | snv | 0.39 | 3 | ||
rs10494879 | 0.925 | 0.120 | 1 | 206778859 | intron variant | C/A;G | snv | 0.36 | 3 | ||
rs1057519833 | 0.925 | 0.120 | 7 | 148809375 | missense variant | G/C | snv | 3 | |||
rs11466782 | 0.925 | 0.120 | 5 | 157494947 | intron variant | A/G | snv | 0.10 | 3 | ||
rs1257715362 | 0.925 | 0.120 | 4 | 85995065 | missense variant | A/G | snv | 7.0E-06 | 3 | ||
rs1351687973 | 0.925 | 0.120 | 1 | 3731497 | missense variant | G/A | snv | 1.6E-05 | 3 | ||
rs138228187 | 0.925 | 0.120 | 11 | 126292650 | missense variant | C/T | snv | 4.0E-05 | 1.4E-05 | 3 | |
rs1555525126 | 0.925 | 0.120 | 17 | 7673749 | missense variant | T/C | snv | 3 | |||
rs2466571 | 0.925 | 0.120 | 1 | 207766701 | intron variant | G/T | snv | 0.46 | 3 | ||
rs535311760 | 0.925 | 0.120 | 1 | 3730979 | missense variant | G/A | snv | 1.2E-05; 8.2E-06 | 3 | ||
rs707824 | 0.925 | 0.120 | 6 | 14636732 | intergenic variant | T/C | snv | 0.74 | 3 | ||
rs708486 | 0.925 | 0.120 | 14 | 52274253 | intron variant | A/G | snv | 0.35 | 3 | ||
rs867329357 | 0.925 | 0.120 | 13 | 102872275 | missense variant | G/A | snv | 4.0E-06 | 4.9E-05 | 3 | |
rs867830180 | 0.925 | 0.120 | 20 | 63695147 | missense variant | G/A;T | snv | 3 |