ZNF208, zinc finger protein 208, 7757

N. diseases: 11; N. variants: 4
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: rs2188971
rs2188971
0.925 0.080 19 21969380 3 prime UTR variant T/A;C snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2188971
rs2188971
0.925 0.080 19 21969380 3 prime UTR variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2188972
rs2188972
1.000 0.080 19 21966656 3 prime UTR variant A/G snv 0.34
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7248488
rs7248488
0.851 0.160 19 22005907 intron variant A/C snv 0.59
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs7248488
rs7248488
0.851 0.160 19 22005907 intron variant A/C snv 0.59
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7248488
rs7248488
0.851 0.160 19 22005907 intron variant A/C snv 0.59
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs7248488
rs7248488
0.851 0.160 19 22005907 intron variant A/C snv 0.59
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs7248488
rs7248488
0.851 0.160 19 22005907 intron variant A/C snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs8103163
rs8103163
0.882 0.120 19 21991950 intron variant A/C snv 0.59
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs8103163
rs8103163
0.882 0.120 19 21991950 intron variant A/C snv 0.59
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs8103163
rs8103163
0.882 0.120 19 21991950 intron variant A/C snv 0.59
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs8103163
rs8103163
0.882 0.120 19 21991950 intron variant A/C snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017