Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.889 5 2009 2020
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.880 1.000 4 2009 2016
dbSNP: rs2853676
rs2853676
0.667 0.560 5 1288432 intron variant T/A;C snv
CUI: C0017638
Disease: Glioma
Glioma
0.840 1.000 2 2009 2017
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.840 1.000 1 2008 2019
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.810 1.000 1 2013 2014
dbSNP: rs2853677
rs2853677
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.810 1.000 1 2012 2016
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.800 1.000 3 2010 2015
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2019
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
0.800 1.000 1 2013 2017
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.800 1.000 1 2009 2014
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.750 1.000 3 2011 2019
dbSNP: rs2242652
rs2242652
0.724 0.400 5 1279913 intron variant G/A snv 0.18
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.710 1.000 1 2011 2013
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
Malignant Testicular Germ Cell Tumor
0.700 1.000 1 2010 2010
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.700 1.000 1 2013 2013
dbSNP: rs2736098
rs2736098
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22
Prostate specific antigen measurement
0.700 1.000 1 2010 2010
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
Malignant Testicular Germ Cell Tumor
0.700 1.000 1 2010 2010
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs2853672
rs2853672
0.882 0.080 5 1292868 intron variant C/A;G snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.700 1.000 1 2013 2013
dbSNP: rs2853676
rs2853676
0.667 0.560 5 1288432 intron variant T/A;C snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs2853676
rs2853676
0.667 0.560 5 1288432 intron variant T/A;C snv
Malignant Testicular Germ Cell Tumor
0.700 1.000 1 2010 2010
dbSNP: rs2853676
rs2853676
0.667 0.560 5 1288432 intron variant T/A;C snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.700 1.000 1 2013 2013