Source: CURATED

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: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 1.000 0 2008 2008
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C2675071
Disease: HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 		0.700 0
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: rs920915
rs920915
ALDH1A2
1.000 0.040 15 58396268 intron variant C/G snv 0.55
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.810 1.000 1 2013 2019
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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
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: 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: rs35853021
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.720 1.000 1 2009 2013
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
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.710 1.000 1 2016 2019
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: rs4471613
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.710 1.000 1 2015 2015
dbSNP: rs10152202
rs10152202
LIPC ; ALDH1A2 ; LIPC-AS1
15 58452149 intron variant T/G snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
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: 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: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs10518976
rs10518976
LIPC ; ALDH1A2 ; LIPC-AS1
15 58459002 intron variant T/A snv 7.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
15 58431227 intron variant A/G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
15 58431227 intron variant A/G snv 0.34
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2013 2013