Source: GWASCAT

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: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 8 2009 2019
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2012 2019
dbSNP: rs261291
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 5 2015 2019
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2010 2019
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2009 2018
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2008 2019
dbSNP: rs16940212
rs16940212
ALDH1A2
1.000 0.040 15 58401821 intron variant G/A;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2011 2019
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2012 2018
dbSNP: rs261291
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2018
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2009 2009
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2012 2012
dbSNP: rs16939881
rs16939881
AQP9 ; ALDH1A2
15 58179780 intron variant G/C;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs16940212
rs16940212
ALDH1A2
1.000 0.040 15 58401821 intron variant G/A;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs261291
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs261291
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		0.710 1.000 1 2013 2015
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0021831
Disease: Intestinal Diseases
Intestinal Diseases 		0.700 1.000 1 2013 2013
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.820 0.667 1 2013 2016
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases 		0.700 1.000 1 2013 2013
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0012242
Disease: Digestive System Disorders
Digestive System Disorders 		0.700 1.000 1 2013 2013