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: rs1077834
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 5 2010 2019
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
15 58431227 intron variant A/G snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 5 2015 2019
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2017 2018
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2019
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: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11631342
rs11631342
LIPC ; ALDH1A2
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs12914626
rs12914626
LIPC ; ALDH1A2 ; LIPC-AS1
1.000 0.040 15 58446224 intron variant C/T snv 0.54
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs17269348
rs17269348
LIPC
0.925 0.040 15 58532442 intron variant A/G snv 7.8E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs17269348
rs17269348
LIPC
0.925 0.040 15 58532442 intron variant A/G snv 7.8E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		0.700 1.000 1 2016 2016
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016