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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.776 | 0.200 | 19 | 46756793 | missense variant | C/T | snv | 9.0E-06 | 0.800 | 1.000 | 6 | 2001 | 2010 | ||||
|
3 | 0.882 | 0.160 | 19 | 46756814 | missense variant | C/A;T | snv | 4.5E-06 | 0.710 | 1.000 | 6 | 2001 | 2008 | ||||
|
2 | 1.000 | 0.120 | 19 | 46756376 | missense variant | A/G | snv | 6.3E-06 | 0.700 | 1.000 | 5 | 2001 | 2007 | ||||
|
4 | 0.882 | 0.160 | 19 | 46756837 | missense variant | A/G | snv | 1.2E-04 | 2.1E-05 | 0.700 | 1.000 | 5 | 2001 | 2007 | |||
|
1 | 1.000 | 0.120 | 19 | 46756651 | missense variant | G/A | snv | 0.700 | 1.000 | 5 | 2001 | 2007 | |||||
|
1 | 1.000 | 0.120 | 19 | 46756113 | missense variant | C/A | snv | 0.700 | 1.000 | 5 | 2001 | 2007 | |||||
|
1 | 1.000 | 0.120 | 19 | 46756663 | missense variant | G/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 5 | 2001 | 2007 | ||||
|
37 | 0.752 | 0.160 | 19 | 46756276 | missense variant | C/A;T | snv | 1.0E-03 | 0.710 | 1.000 | 1 | 2001 | 2001 | ||||
|
1 | 1.000 | 0.120 | 19 | 46756844 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 19 | 46755791 | missense variant | C/G | snv | 1.0E-02 | 9.0E-03 | 0.700 | 0 | ||||||
|
6 | 0.827 | 0.160 | 19 | 46755995 | missense variant | A/G;T | snv | 8.2E-05; 6.8E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 19 | 46756397 | missense variant | C/G | snv | 6.0E-06 | 7.0E-06 | 0.700 | 0 |