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: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2008 2019
dbSNP: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2008 2009
dbSNP: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11668477
rs11668477 		0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		0.700 1.000 1 2012 2012