DisGeNET - a database of gene-disease associations

CYP4F3, cytochrome P450 family 4 subfamily F member 3, 4051

N. diseases: 114; N. variants: 13

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs10401516

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs2072598

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs2077040

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs2077080

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs2203999

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs2204000

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs4808346

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs8106799

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0523465
Disease:

Serum albumin measurement

0.700

GeneticVariation

GWASDB

A genome-wide assessment of variability in human serum metabolism.

23281178

2013

dbSNP:

rs4646904

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0684249
Disease:

Carcinoma of lung

0.010

GeneticVariation

BEFREE

The results suggest that a potentially functional SNP in CYP4F3 (rs4646904) may contribute to the etiology of lung cancer, especially in smokers.

28150878

2017

dbSNP:

rs4646904

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C1306460
Disease:

Primary malignant neoplasm of lung

0.010

GeneticVariation

BEFREE

The results suggest that a potentially functional SNP in CYP4F3 (rs4646904) may contribute to the etiology of lung cancer, especially in smokers.

28150878

2017

dbSNP:

rs4646904

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0242379
Disease:

Malignant neoplasm of lung

0.010

GeneticVariation

BEFREE

The results suggest that a potentially functional SNP in CYP4F3 (rs4646904) may contribute to the etiology of lung cancer, especially in smokers.

28150878

2017

dbSNP:

rs554326805

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0007131
Disease:

Non-Small Cell Lung Carcinoma

0.010

GeneticVariation

BEFREE

In this study, CYP1A1 (Ile462Val), CYP1B1(Asn453Ser), GST M1, GSTP1 exon 5 (Ile105Val) and exon 6(Ala114Val) and GSTT1 polymorphisms were determined in 138 patients with advanced NSCLC to evaluate their role in survival.

20845989

2010

dbSNP:

rs749777680

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0007131
Disease:

Non-Small Cell Lung Carcinoma

0.010

GeneticVariation

BEFREE

20845989

2010

dbSNP:

rs780092348

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0007131
Disease:

Non-Small Cell Lung Carcinoma

0.010

GeneticVariation

BEFREE

20845989

2010

dbSNP:

rs945232586

Entrez Id:	4051
Gene Symbol:	CYP4F3

CYP4F3

CUI:	C0392702
Disease:

Abnormal involuntary movement

0.010

GeneticVariation

BEFREE

Interactive effects of cytochrome P 450 17alpha-hydroxylase with the dopamine D3 Ser9Gly polymorphism on abnormal involuntary movements were examined.

11839369

2002