Source: ALL
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: rs2338104
rs2338104 		1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2008 2019
dbSNP: rs2338104
rs2338104 		1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2008 2009
dbSNP: rs2058804
rs2058804 		12 109471206 missense variant A/C;G snv 0.50
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2338104
rs2338104 		1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4766601
rs4766601 		12 109452275 intron variant G/C snv 0.21
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11066782
rs11066782 		1.000 0.040 12 109472747 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11066782
rs11066782 		1.000 0.040 12 109472747 intron variant C/T snv 0.17
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11613718
rs11613718 		1.000 0.040 12 109474527 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11613718
rs11613718 		1.000 0.040 12 109474527 intron variant C/T snv 0.17
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs56209061
rs56209061 		1.000 0.040 12 109467880 intron variant G/A snv 4.7E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2019 2019