Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 8 | 118947384 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1 | 8 | 118936926 | intron variant | T/C | snv | 0.45 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 8 | 118942040 | intron variant | G/A | snv | 0.60 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
2 | 1.000 | 0.040 | 8 | 118939453 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
9 | 0.776 | 0.360 | 8 | 118952044 | upstream gene variant | G/A | snv | 0.58 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
19 | 0.716 | 0.480 | 8 | 118951813 | missense variant | G/C | snv | 0.52 | 0.60 | 0.700 | 1.000 | 1 | 2009 | 2009 | |||
|
1 | 8 | 118947418 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1 | 8 | 118935412 | intron variant | A/G | snv | 0.33 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 8 | 118942872 | intron variant | G/A | snv | 0.67 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 8 | 118940511 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1 | 8 | 118948422 | intron variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1 | 8 | 118934417 | intron variant | C/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 8 | 118945386 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1 | 8 | 118942603 | intron variant | T/C | snv | 0.60 | 0.700 | 1.000 | 1 | 2009 | 2009 |