Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2004640 | 0.662 | 0.520 | 7 | 128938247 | splice donor variant | T/G | snv | 0.52 | 26 | ||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 21 | ||
rs185819 | 0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 | 10 | ||
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 9 | ||
rs3823418 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 0.23 | 8 | ||
rs2844479 | 0.925 | 0.200 | 6 | 31605179 | intergenic variant | A/C | snv | 0.34 | 5 | ||
rs6457620 | 0.882 | 0.200 | 6 | 32696222 | intergenic variant | G/C | snv | 0.52 | 5 | ||
rs537160 | 0.882 | 0.240 | 6 | 31948623 | intron variant | A/G | snv | 0.73 | 4 | ||
rs2261033 | 0.925 | 0.160 | 6 | 31635814 | non coding transcript exon variant | A/G | snv | 0.42 | 3 | ||
rs2857693 | 1.000 | 0.120 | 6 | 31620607 | upstream gene variant | G/T | snv | 0.33 | 2 | ||
rs6930571 | 1.000 | 0.120 | 6 | 32415431 | regulatory region variant | G/T | snv | 0.13 | 2 |