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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
22 | 36295526 | missense variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.800 | 1.000 | 11 | 2000 | 2006 | ||||||||||
|
22 | 36295650 | missense variant | A/G | snv | 3.2E-04 | 4.3E-04 |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 11 | 2000 | 2006 | ||||||||
|
22 | 36300961 | missense variant | T/G | snv | 1.6E-04 | 2.8E-05 |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 11 | 2000 | 2006 | ||||||||
|
22 | 36285158 | missense variant | T/C | snv | 1.6E-05 | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 11 | 2000 | 2006 | ||||||||
|
22 | 36292132 | missense variant | G/A | snv | 1.0E-03 | 1.2E-03 |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 11 | 2000 | 2006 | ||||||||
|
22 | 36362502 | intron variant | A/G | snv | 0.62 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
22 | 36286661 | intron variant | G/A | snv | 5.7E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
22 | 36362502 | intron variant | A/G | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
22 | 36284668 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
22 | 36375211 | intron variant | G/C | snv | 4.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 36336957 | intron variant | A/G | snv | 4.4E-04 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
22 | 36282730 | frameshift variant | C/- | delins |
|
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | 22 | 36281936 | 3 prime UTR variant | G/A;T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 22 | 36281936 | 3 prime UTR variant | G/A;T | snv |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 22 | 36281936 | 3 prime UTR variant | G/A;T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 22 | 36316427 | intron variant | A/G | snv | 0.90 |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 22 | 36316427 | intron variant | A/G | snv | 0.90 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.080 | 22 | 36299382 | intron variant | C/T | snv | 0.78 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.020 | 1.000 | 2 | 2009 | 2012 | |||||||
|
0.882 | 0.080 | 22 | 36299382 | intron variant | C/T | snv | 0.78 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.080 | 22 | 36299382 | intron variant | C/T | snv | 0.78 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.080 | 22 | 36312039 | intron variant | C/G;T | snv | 0.88 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.080 | 22 | 36312039 | intron variant | C/G;T | snv | 0.88 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 22 | 36299896 | intron variant | C/T | snv | 0.78 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.080 | 22 | 36285296 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||
|
1.000 | 0.080 | 22 | 36285296 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.700 | 0 |