PLPP3, phospholipid phosphatase 3, 8613

N. diseases: 8; N. variants: 13
Source: GWASCAT ×
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: rs17114036
rs17114036 		0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 2 2011 2014
dbSNP: rs17114046
rs17114046 		0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 2 2011 2011
dbSNP: rs17114046
rs17114046 		0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs11206830
rs11206830 		1.000 0.120 1 56494451 intron variant C/T snv 8.7E-02
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs147055617
rs147055617 		1.000 0.040 1 56520631 intron variant A/G snv 8.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17114036
rs17114036 		0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs17416285
rs17416285 		1.000 0.040 1 56554977 intron variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2404715
rs2404715 		1.000 0.040 1 56543106 intron variant C/T snv 7.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs4634932
rs4634932 		1.000 0.040 1 56530519 intron variant T/C snv 7.2E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs55869368
rs55869368 		1 56520961 intron variant C/A;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs56170783
rs56170783 		1.000 0.040 1 56550459 intron variant A/C snv 6.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs61772626
rs61772626 		1 56549996 intron variant A/G snv 0.11
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs72664324
rs72664324 		1.000 0.040 1 56506681 intron variant G/A snv 0.10
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs75264190
rs75264190 		1 56553312 intron variant C/T snv 9.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs9970807
rs9970807 		0.925 0.080 1 56499992 intron variant C/T snv 0.11
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs9970807
rs9970807 		0.925 0.080 1 56499992 intron variant C/T snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2015 2015