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: 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: rs13329672
rs13329672
ALDH1A2
15 58407738 intron variant C/T snv 0.31
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2018 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: 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: 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: rs7350789
rs7350789
ALDH1A2
15 58387469 intron variant G/A snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2018
dbSNP: rs7350789
rs7350789
ALDH1A2
15 58387469 intron variant G/A snv 0.35
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2019
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: 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: rs118146059
rs118146059
ALDH1A2
15 58252574 intron variant T/C snv 1.7E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12148399
rs12148399
ALDH1A2
15 58289171 intron variant T/A snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12148399
rs12148399
ALDH1A2
15 58289171 intron variant T/A snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12148780
rs12148780
ALDH1A2
1.000 0.080 15 58289090 intron variant A/G snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs12148780
rs12148780
ALDH1A2
1.000 0.080 15 58289090 intron variant A/G snv 0.14
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs12903590
rs12903590
ALDH1A2
15 58285578 intron variant A/T snv 0.15
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		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: rs13329672
rs13329672
ALDH1A2
15 58407738 intron variant C/T snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13329672
rs13329672
ALDH1A2
15 58407738 intron variant C/T snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 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