CCNA2, cyclin A2, 890

N. diseases: 90; N. variants: 5
Source: ALL
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.
dbSNP: rs3217772
rs3217772
4 121818028 intron variant C/G snv 0.37; 1.2E-05 0.29
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3762840
rs3762840
4 121825441 3 prime UTR variant A/T snv 0.29
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs769246
rs769246
4 121820188 intron variant A/G;T snv
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs769246
rs769246
4 121820188 intron variant A/G;T snv
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs768000961
rs768000961
4 121823490 missense variant G/A snv 8.1E-06
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs769236
rs769236
0.882 0.080 4 121823883 5 prime UTR variant C/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs769236
rs769236
0.882 0.080 4 121823883 5 prime UTR variant C/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs769236
rs769236
0.882 0.080 4 121823883 5 prime UTR variant C/A;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011