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: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.900 1.000 1 2010 2020
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.900 1.000 1 2005 2019
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.880 1.000 1 2001 2019
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes 		0.800 1.000 2 2011 2013
dbSNP: rs2238151
rs2238151
ALDH2
1.000 0.040 12 111774029 intron variant T/C snv 0.52
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.800 1.000 1 2012 2012
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 1.000 1 2013 2017
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.780 1.000 2 2001 2019
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.710 1.000 1 2011 2019
dbSNP: rs11066028
rs11066028
ALDH2
1.000 0.080 12 111807366 intron variant A/C snv 0.45
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4646776
rs4646776
ALDH2
0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes 		0.700 1.000 1 2013 2013
dbSNP: rs4646776
rs4646776
ALDH2
0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.700 1.000 1 2011 2011
dbSNP: rs4648328
rs4648328
ALDH2
12 111784984 intron variant C/T snv 0.18
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2014 2014
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2014 2014
dbSNP: rs671
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010