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: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 6 2009 2013
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 6 2009 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: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2009 2012
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2009 2019
dbSNP: rs4775041
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2008 2012
dbSNP: rs4775041
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2008 2019
dbSNP: rs4775041
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 3 2008 2013
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.890 0.900 2 2010 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 2 2010 2019
dbSNP: rs17821159
rs17821159
ALDH1A2
15 58264863 intron variant A/G snv 0.32
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs2043085
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs4775041
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2008 2018
dbSNP: rs493258
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.860 1.000 2 2010 2019
dbSNP: rs10152355
rs10152355
ALDH1A2
15 58378979 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2009 2018
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs11071377
rs11071377
ALDH1A2
15 58385196 intron variant A/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11852978
rs11852978
ALDH1A2
15 58406556 intron variant T/G snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11853674
rs11853674
ALDH1A2
15 58391858 intron variant A/G snv 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012