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: rs261334
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
15 58434545 intron variant G/C snv 0.73
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2010 2019
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
15 58431227 intron variant A/G snv 0.34
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2013 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: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
15 58438954 intron variant G/A;C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
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: rs8034802
rs8034802
LIPC ; ALDH1A2
15 58432593 intron variant T/A snv 0.33
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2011 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: 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: 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: 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: 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: 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