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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 12 | 4372733 | non coding transcript exon variant | -/A;G | ins | 4.0E-06; 0.12; 4.0E-06; 4.0E-06 | 0.10 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
7 | 0.882 | 0.160 | 2 | 210675762 | missense variant | A/C | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
10 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 10 | 17138170 | 3 prime UTR variant | A/C | snv | 0.51 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.100 | 1.000 | 13 | 2001 | 2019 | |||
|
101 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 0.040 | 1.000 | 4 | 2006 | 2017 | |||
|
135 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
6 | 0.851 | 0.120 | 1 | 118360355 | intergenic variant | A/G | snv | 0.25 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 11 | 67579946 | upstream gene variant | A/G | snv | 0.38 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
3 | 0.925 | 0.120 | 19 | 18868625 | missense variant | A/G | snv | 5.1E-04 | 2.7E-04 | 0.700 | 0 | ||||||
|
214 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 0.020 | 1.000 | 2 | 2011 | 2013 | ||||
|
1 | 14 | 27023434 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
3 | 1.000 | 0.080 | 8 | 11755064 | missense variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 12 | 16349610 | intron variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
4 | 0.925 | 0.120 | 12 | 119876131 | frameshift variant | AAAGGATTCC/- | delins | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.120 | 20 | 10645245 | frameshift variant | ACTG/- | delins | 0.700 | 1.000 | 4 | 1997 | 2005 | |||||
|
10 | 0.763 | 0.200 | 16 | 331927 | intron variant | C/A | snv | 0.18 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 15 | 79885941 | intron variant | C/A;T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 6 | 42960279 | upstream gene variant | C/G | snv | 0.41 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 14 | 40807221 | intron variant | C/G | snv | 0.19 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
2 | 14 | 23413792 | missense variant | C/G | snv | 7.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 21 | 43076866 | 5 prime UTR variant | C/G | snv | 0.88 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
6 | 0.882 | 0.120 | 12 | 114385521 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
7 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
5 | 0.925 | 0.120 | 12 | 114401830 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 |