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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
12 | 123975620 | intron variant | G/T | snv | 0.33 |
|
0.800 | 1.000 | 4 | 2010 | 2019 | ||||||||||
|
1.000 | 0.040 | 12 | 123996254 | intron variant | A/G | snv | 0.17 |
|
Mental Disorders | 0.700 | 1.000 | 3 | 2015 | 2019 | |||||||
|
12 | 123975620 | intron variant | G/T | snv | 0.33 |
|
0.800 | 1.000 | 3 | 2010 | 2018 | ||||||||||
|
12 | 123975620 | intron variant | G/T | snv | 0.33 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||||
|
12 | 123980289 | intron variant | G/T | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
12 | 124004615 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
12 | 124100790 | intron variant | G/A | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124267534 | intron variant | C/T | snv | 3.9E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124293085 | intron variant | G/A | snv | 0.61 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124006982 | intron variant | G/C | snv | 0.60 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
12 | 124002131 | intron variant | A/G | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124019257 | intron variant | AA/-;A;AAA | delins | 0.49 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 12 | 124120741 | intron variant | A/G | snv | 0.71 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
12 | 123990609 | intron variant | A/G | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 123990609 | intron variant | A/G | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 12 | 124129992 | intron variant | T/C | snv | 0.23 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.710 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 12 | 124083909 | intron variant | C/T | snv | 0.51 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.120 | 12 | 124083909 | intron variant | C/T | snv | 0.51 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
12 | 124020897 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |