Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.160 | 3 | 41922636 | intron variant | G/A;C;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.160 | 3 | 41829905 | intron variant | A/C;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.160 | 3 | 41890838 | intron variant | G/A | snv | 0.11 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.160 | 3 | 41872124 | intron variant | G/A;C;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.160 | 3 | 41946428 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
3 | 41376349 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
3 | 41269871 | intron variant | G/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.851 | 0.160 | 3 | 41709497 | intron variant | T/C | snv | 0.30 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.160 | 3 | 41871159 | intron variant | G/A;T | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.160 | 3 | 41871159 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 3 | 2009 | 2017 | |||||||||
|
1.000 | 0.160 | 3 | 41946428 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
1.000 | 0.160 | 3 | 41954644 | missense variant | T/C | snv | 0.79 | 0.67 |
|
0.700 | 1.000 | 2 | 2016 | 2016 | |||||||
|
3 | 41841413 | intron variant | G/C | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
3 | 41827229 | intron variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.160 | 3 | 41922636 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.160 | 3 | 41873406 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.160 | 3 | 41872124 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.160 | 3 | 41948630 | intron variant | G/A | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.160 | 3 | 41929251 | intron variant | T/C | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.160 | 3 | 41724463 | intron variant | A/G | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
3 | 41880318 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.160 | 3 | 41929251 | intron variant | T/C | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
3 | 41880318 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |