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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 0.900 | 0.950 | 9 | 2009 | 2019 | ||||
|
29 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 0.890 | 0.933 | 6 | 2005 | 2019 | |||
|
23 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 0.720 | 1.000 | 3 | 2011 | 2019 | |||
|
1 | 1.000 | 0.080 | 19 | 44909698 | non coding transcript exon variant | A/C | snv | 3.0E-02 | 0.700 | 1.000 | 2 | 2018 | 2019 | ||||
|
1 | 0.925 | 0.120 | 19 | 44904531 | upstream gene variant | G/A;C | snv | 0.800 | 1.000 | 2 | 2013 | 2019 | |||||
|
10 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 0.700 | 1.000 | 2 | 2013 | 2019 | ||||
|
1 | 0.925 | 0.120 | 19 | 44905307 | upstream gene variant | A/T | snv | 0.21 | 0.730 | 1.000 | 1 | 2009 | 2018 | ||||
|
4 | 0.882 | 0.120 | 19 | 44905371 | upstream gene variant | T/C | snv | 7.0E-02 | 0.740 | 1.000 | 1 | 2009 | 2018 | ||||
|
4 | 0.925 | 0.120 | 19 | 44907187 | non coding transcript exon variant | G/A | snv | 0.39 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.160 | 19 | 44907853 | missense variant | T/C | snv | 2.5E-03 | 1.9E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 |