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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 74261866 | intron variant | T/C | snv | 0.48 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
10 | 74603349 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 74683339 | intron variant | A/G | snv | 0.68 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
10 | 74287706 | intron variant | C/T | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.120 | 10 | 74640406 | intron variant | C/T | snv | 0.27 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
10 | 74226399 | intron variant | C/T | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.040 | 10 | 74272653 | intron variant | A/C | snv | 4.7E-02 |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.040 | 10 | 74272653 | intron variant | A/C | snv | 4.7E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 10 | 74394294 | missense variant | T/C | snv | 8.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 10 | 74394294 | missense variant | T/C | snv | 8.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 10 | 74670258 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 10 | 74525404 | missense variant | A/C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
1.000 | 10 | 74200787 | missense variant | G/A | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
1.000 | 10 | 74670258 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 10 | 74670258 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 10 | 74670258 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 10 | 74670258 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.040 | 10 | 74176853 | 5 prime UTR variant | C/G;T | snv | 0.67 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.040 | 10 | 74176853 | 5 prime UTR variant | C/G;T | snv | 0.67 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |