PLA2G4A, phospholipase A2 group IVA, 5321

N. diseases: 202; N. variants: 15
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: rs10798069
rs10798069 		1.000 0.040 1 186906327 intron variant G/T snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs10798069
rs10798069 		1.000 0.040 1 186906327 intron variant G/T snv 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs12720690
rs12720690 		1 186979089 intron variant G/T snv 2.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6672835
rs6672835 		1 186971624 intron variant A/T snv 0.96
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs6674263
rs6674263 		1 186967030 intron variant A/T snv 0.96
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs121434634
rs121434634 		1.000 1 186894164 missense variant T/C snv
CUI: C3888207
Disease: PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF
PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF 		0.700 0
dbSNP: rs121434635
rs121434635 		1.000 1 186956219 missense variant G/A snv
CUI: C3888207
Disease: PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF
PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF 		0.700 0
dbSNP: rs1557895416
rs1557895416 		1.000 1 186965552 missense variant G/C snv
CUI: C3888207
Disease: PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF
PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF 		0.700 0
dbSNP: rs1557901999
rs1557901999 		1.000 1 186979473 splice region variant AGTA/- delins
CUI: C3888207
Disease: PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF
PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF 		0.700 0
dbSNP: rs370896190
rs370896190 		1.000 0.080 1 186950718 missense variant C/G;T snv 1.1E-04
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs10798059
rs10798059 		0.925 0.080 1 186830478 intron variant G/A snv 0.40
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.030 0.667 3 2009 2019
dbSNP: rs10798059
rs10798059 		0.925 0.080 1 186830478 intron variant G/A snv 0.40
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C0042109
Disease: Urticaria
Urticaria 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C3845502
Disease: Myocardial infarction, stroke
Myocardial infarction, stroke 		0.010 1.000 1 2011 2011
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs12746200
rs12746200 		0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02
CUI: C0741923
Disease: cardiac event
cardiac event 		0.010 1.000 1 2011 2011
dbSNP: rs3820185
rs3820185 		1.000 0.120 1 186839211 intron variant G/T snv 0.36
CUI: C1868001
Disease: Polyposis Of Gastric Fundus Without Polyposis Coli
Polyposis Of Gastric Fundus Without Polyposis Coli 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs4650708
rs4650708 		1.000 0.080 1 186940985 intron variant A/C snv 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs6666834
rs6666834 		1.000 0.080 1 186936689 intron variant C/T snv 0.31
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs7526089
rs7526089 		1.000 0.080 1 186983499 intron variant C/T snv 0.23
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012