DisGeNET - a database of gene-disease associations

rs773919809, MGMT

N. diseases: 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

Disease

N. SNPs_d

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

Malignant Neoplasms

CUI:	C0006826
Disease:	Malignant Neoplasms

1641

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.030

0.667

2007

2013

Primary malignant neoplasm

CUI:	C1306459
Disease:	Primary malignant neoplasm

1374

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.030

0.667

2007

2013

Squamous cell carcinoma of esophagus

CUI:	C0279626
Disease:	Squamous cell carcinoma of esophagus

329

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.030

1.000

2008

2012

Neoplasms

CUI:	C0027651
Disease:	Neoplasms

1644

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.020

0.500

2007

2013

cervical cancer

CUI:	C4048328
Disease:	cervical cancer

268

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

2005

2005

Colorectal Carcinoma

CUI:	C0009402
Disease:	Colorectal Carcinoma

1962

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2006

2006

Glioma

CUI:	C0017638
Disease:	Glioma

353

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2013

2013

Lymphoma

CUI:	C0024299
Disease:	Lymphoma

91

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2004

2004

Malignant neoplasm of colon and/or rectum

CUI:	C4722085
Disease:	Malignant neoplasm of colon and/or rectum

502

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2006

2006

Malignant neoplasm of stomach

CUI:	C0024623
Disease:	Malignant neoplasm of stomach

615

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2014

2014

Methylenetetrahydrofolate reductase polymorphism

CUI:	C2721734
Disease:	Methylenetetrahydrofolate reductase polymorphism

7

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2013

2013

Squamous cell carcinoma of skin

CUI:	C0553723
Disease:	Squamous cell carcinoma of skin

92

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2010

2010

Stomach Carcinoma

CUI:	C0699791
Disease:	Stomach Carcinoma

652

0.763

0.200

10

129766957

missense variant

C/T

snv

2.0E-05

0.010

1.000

2014

2014