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: 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 8 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: 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 4 2010 2019
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: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2009 2009
dbSNP: rs1532085
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
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