CDKN1A, cyclin dependent kinase inhibitor 1A, 1026

N. diseases: 490; N. variants: 17
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: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2015 2015
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2015 2015
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma
Neoplasms; Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs1236971182
rs1236971182
1.000 0.080 6 36684381 missense variant C/T snv 8.1E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 1996 1996
dbSNP: rs1276639827
rs1276639827
6 36684171 missense variant C/T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs1276639827
rs1276639827
6 36684171 missense variant C/T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2010 2010
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2015 2015
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0153560
Disease: Kaposi's sarcoma of skin
Kaposi's sarcoma of skin
Neoplasms; Infections 0.010 1.000 1 2011 2011
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 1995 1995
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2013 2013
dbSNP: rs2395655
rs2395655
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2395655
rs2395655
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3176336
rs3176336
0.925 0.080 6 36681039 intron variant A/T snv 0.54
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs3176336
rs3176336
0.925 0.080 6 36681039 intron variant A/T snv 0.54
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs3176352
rs3176352
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012