Source: GWASDB

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: rs487766
rs487766
ALDH1A2
15 58401661 intron variant C/T snv 0.73
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs487766
rs487766
ALDH1A2
15 58401661 intron variant C/T snv 0.73
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2011 2011
dbSNP: rs487766
rs487766
ALDH1A2
15 58401661 intron variant C/T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs487766
rs487766
ALDH1A2
15 58401661 intron variant C/T snv 0.73
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2011 2011