DisGeNET - a database of gene-disease associations

Source: ALL

Variant: rs121913361 ×

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

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF _EXOME

AF _GENOME

Disease

Score _vda

EI _vda

N_.PMIDs

FirstRef.

LastRef.

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0009404
Disease:	Colorectal Neoplasms

Colorectal Neoplasms

0.700

1.000

2002

2014

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0017636
Disease:	Glioblastoma

Glioblastoma

0.700

1.000

2016

2016

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0026764
Disease:	Multiple Myeloma

Multiple Myeloma

0.700

1.000

2016

2016

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0279680
Disease:	Transitional cell carcinoma of bladder

Transitional cell carcinoma of bladder

0.700

1.000

2016

2016

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0152013
Disease:	Adenocarcinoma of lung (disorder)

Adenocarcinoma of lung (disorder)

0.700

1.000

2016

2016

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C0025202
Disease:	melanoma

melanoma

0.700

1.000

2014

2014

dbSNP:

rs121913361

rs121913361

BRAF

0.807

0.280

7

140753349

missense variant

C/A;G;T

snv

CUI:	C1319315
Disease:	Adenocarcinoma of large intestine

Adenocarcinoma of large intestine

0.700