rs10204525, PDCD1

N. diseases: 20
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.040 1.000 4 2014 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.020 1.000 2 2015 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.020 1.000 2 2015 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.020 0.500 2 2014 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.020 0.500 2 2014 2016
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.020 1.000 2 2014 2016
Acute anterior uveitis
CUI: C0701807
Disease: Acute anterior uveitis
30 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2013 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2011 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
Elephantiasis
CUI: C0013882
Disease: Elephantiasis
6 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
Filarial Elephantiases
CUI: C0013884
Disease: Filarial Elephantiases
10 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
Hepatitis, Chronic
CUI: C0019189
Disease: Hepatitis, Chronic
10 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2015 2015
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016