Source: GWASDB ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7120118
rs7120118 		0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2009 2012
dbSNP: rs10838681
rs10838681 		1.000 0.040 11 47253513 intron variant G/A snv 0.34
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.800 1.000 1 2012 2012
dbSNP: rs7120118
rs7120118 		0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.710 1.000 1 2011 2016
dbSNP: rs7120118
rs7120118 		0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2009 2012
dbSNP: rs2279238
rs2279238 		0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2279238
rs2279238 		0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012