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: rs3176326
rs3176326
1.000 0.080 6 36679512 intron variant G/A snv 0.20
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs2395655
rs2395655
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2395655
rs2395655
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs3176336
rs3176336
0.925 0.080 6 36681039 intron variant A/T snv 0.54
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3176353
rs3176353
6 36684828 intron variant C/T snv 3.2E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs3176353
rs3176353
6 36684828 intron variant C/T snv 3.2E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3829964
rs3829964
1.000 0.080 6 36676721 intron variant T/C snv 0.60
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs762624
rs762624
0.851 0.280 6 36677811 non coding transcript exon variant A/C;T snv 0.37; 2.4E-05
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs762624
rs762624
0.851 0.280 6 36677811 non coding transcript exon variant A/C;T snv 0.37; 2.4E-05
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.040 1.000 4 2005 2015
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.040 1.000 4 2005 2015
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.040 1.000 4 2005 2015
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.040 1.000 4 2005 2015
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma
Neoplasms; Eye Diseases 0.030 1.000 3 2013 2018
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.030 1.000 3 1995 2016
dbSNP: rs2395655
rs2395655
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.030 1.000 3 2014 2019
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
Squamous cell carcinoma of the head and neck
Neoplasms 0.020 1.000 2 2015 2015
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 0.500 2 2007 2011
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.020 0.500 2 2007 2011
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 0.500 2 2012 2016
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 1997 2006
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 0.500 2 2007 2011
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 0.500 2 2012 2016
dbSNP: rs1801270
rs1801270
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 0.500 2 2012 2016
dbSNP: rs1059234
rs1059234
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012