LBP, lipopolysaccharide binding protein, 3929

N. diseases: 156; N. variants: 7
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: rs1780617
rs1780617 		20 38345754 upstream gene variant G/A snv 0.77
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs2232613
rs2232613 		20 38369011 missense variant C/G;T snv 6.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2232618
rs2232618 		0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2012 2018
dbSNP: rs2232618
rs2232618 		0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2012 2018
dbSNP: rs140189115
rs140189115 		0.925 0.080 20 38360728 missense variant G/A snv 8.0E-06 7.0E-06
CUI: C1541923
Disease: Infective endocarditis
Infective endocarditis 		Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs140189115
rs140189115 		0.925 0.080 20 38360728 missense variant G/A snv 8.0E-06 7.0E-06
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis 		Infections; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2232582
rs2232582 		0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs2232582
rs2232582 		0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22
CUI: C1541923
Disease: Infective endocarditis
Infective endocarditis 		Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2232582
rs2232582 		0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis 		Infections; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2232596
rs2232596 		1.000 0.080 20 38360727 synonymous variant A/G snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs2232618
rs2232618 		0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12
CUI: C0015967
Disease: Fever
Fever 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs2232618
rs2232618 		0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12
CUI: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs2232618
rs2232618 		0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs374520012
rs374520012 		0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs374520012
rs374520012 		0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2001 2001
dbSNP: rs374520012
rs374520012 		0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2001 2001