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 | 14 | 65024537 | intron variant | A/G | snv | 0.58 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 14 | 65020976 | intron variant | T/C | snv | 0.36 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 14 | 65021078 | intron variant | T/C | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 14 | 65043160 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 14 | 65033191 | intron variant | T/G | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 65012230 | non coding transcript exon variant | T/G | snv | 0.13 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 14 | 65008822 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 14 | 65007157 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 14 | 65013877 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
3 | 14 | 65006478 | intron variant | G/A | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
4 | 14 | 65035521 | intron variant | G/A | snv | 0.61 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 65053898 | intron variant | G/A | snv | 0.50 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
2 | 14 | 65029098 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 14 | 65034017 | intron variant | A/G | snv | 0.61 | 0.700 | 1.000 | 1 | 2012 | 2012 |