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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 0.882 | 0.080 | 8 | 38421872 | missense variant | C/A;T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2000 | 2011 | ||||
|
3 | 0.882 | 0.080 | 8 | 38419718 | missense variant | C/A | snv | 4.0E-06 | 0.020 | 1.000 | 2 | 2000 | 2002 | ||||
|
1 | 1.000 | 0.080 | 10 | 121498597 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
1 | 1.000 | 0.080 | 5 | 428121 | intron variant | C/A | snv | 0.27 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
6 | 0.807 | 0.080 | 10 | 121520050 | missense variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
3 | 0.882 | 0.080 | 10 | 121496701 | missense variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
1 | 1.000 | 0.080 | 12 | 10997434 | missense variant | G/T | snv | 0.42 | 0.30 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
1 | 1.000 | 0.080 | 12 | 10997447 | missense variant | G/T | snv | 0.42 | 0.29 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
1 | 1.000 | 0.080 | 10 | 121485399 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.080 | 14 | 70050466 | intron variant | T/C;G | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.080 | 22 | 40409697 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.080 | 11 | 16341047 | missense variant | C/T | snv | 1.3E-03 | 6.8E-04 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
2 | 0.925 | 0.080 | 10 | 121515287 | missense variant | G/A | snv | 3.5E-05 | 0.010 | 1.000 | 1 | 1997 | 1997 | ||||
|
2 | 1.000 | 0.080 | 2 | 102344364 | 3 prime UTR variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
|
1 | 1.000 | 0.080 | 6 | 33312532 | intron variant | C/T | snv | 0.23 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 10 | 77132657 | intron variant | T/C | snv | 0.14 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 4 | 1803761 | missense variant | G/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 0.080 | 2 | 86791424 | 5 prime UTR variant | A/G | snv | 0.20 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 7 | 116697595 | intron variant | G/A | snv | 0.20 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.080 | 7 | 116801535 | downstream gene variant | A/G | snv | 0.34 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.080 | 7 | 36643290 | intron variant | T/C | snv | 0.41 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 72266805 | intron variant | T/C | snv | 0.82 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
2 | 1.000 | 0.080 | 2 | 102351615 | missense variant | T/C;G | snv | 0.34; 4.0E-06 | 0.46 | 0.010 | 1.000 | 1 | 2009 | 2009 | |||
|
1 | 1.000 | 0.080 | 6 | 73174426 | intron variant | C/T | snv | 0.48 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 1 | 192366662 | 3 prime UTR variant | A/C;G;T | snv | 0.010 | < 0.001 | 1 | 2019 | 2019 |