LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
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: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.830 1.000 6 2011 2018
dbSNP: rs3798220
rs3798220 		0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.820 1.000 4 2011 2013
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0428791
Disease: Aortic valve calcification
Aortic valve calcification 		Nutritional and Metabolic Diseases; Cardiovascular Diseases 0.820 1.000 2 2013 2019
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 6 2012 2019
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2012 2019
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.770 0.875 8 2012 2019
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.710 1.000 2 2013 2015
dbSNP: rs10755578
rs10755578 		0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 2 2009 2012
dbSNP: rs41272114
rs41272114 		1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 2 2014 2018
dbSNP: rs7767084
rs7767084 		0.925 0.040 6 160541471 intron variant T/C snv 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.710 1.000 2 2009 2013
dbSNP: rs7767084
rs7767084 		0.925 0.040 6 160541471 intron variant T/C snv 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 2 2009 2012
dbSNP: rs74617384
rs74617384 		0.925 0.080 6 160576086 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 1 2018 2018
dbSNP: rs55730499
rs55730499 		1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 3 2015 2018
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs140570886
rs140570886 		1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2017 2018
dbSNP: rs191555775
rs191555775 		6 160584357 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs55730499
rs55730499 		1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 2 2013 2017
dbSNP: rs73596816
rs73596816 		1.000 0.040 6 160596331 intron variant G/A snv 3.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2018 2019
dbSNP: rs73596816
rs73596816 		1.000 0.040 6 160596331 intron variant G/A snv 3.6E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 2 2017 2019
dbSNP: rs7770628
rs7770628 		1.000 0.040 6 160597142 intron variant C/T snv 0.63
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 2 2017 2019
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C3549252
Disease: response to statin
response to statin 		0.700 1.000 1 2012 2012
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.700 1.000 1 2012 2012
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis 		Infections; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs10455872
rs10455872 		0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.700 1.000 1 2017 2017