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: 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: 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: rs1601935
rs1601935
ALDH1A2
15 58379566 intron variant G/T snv 0.60
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs1601935
rs1601935
ALDH1A2
15 58379566 intron variant G/T snv 0.60
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs1601935
rs1601935
ALDH1A2
15 58379566 intron variant G/T snv 0.60
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
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: rs16940170
rs16940170
ALDH1A2
1.000 0.040 15 58392083 intron variant G/A snv 0.15
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
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: 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: 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: 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: 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: rs187775
rs187775
ALDH1A2
0.925 0.120 15 58385696 intron variant A/T snv 9.6E-02
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 1.000 1 2012 2012
dbSNP: rs187775
rs187775
ALDH1A2
0.925 0.120 15 58385696 intron variant A/T snv 9.6E-02
CUI: C0018099
Disease: Gout
Gout 		0.700 1.000 1 2012 2012
dbSNP: rs2043082
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2043082
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2043082
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs2043082
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2043085
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs2043085
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		0.700 1.000 1 2016 2016
dbSNP: rs2043085
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.710 1.000 1 2016 2019