Gene

BRAF

HGNC: HGNC:1097 | GeneCards: BRAF

None recorded

0ClinVar pathogenic / likely pathogenic

Co-reported phenotypes

Phenotypes named in the same articles as BRAF. Co-mention, not a proven association.

Phenotype	Articles	Evidence
thyroid cancer	54	View sentences
colorectal cancer	29	View sentences
lung cancer	7	View sentences
breast cancer	6	View sentences
ovarian cancer	4	View sentences
cardiomyopathy	2	View sentences
epilepsy	2	View sentences
Down syndrome	1	View sentences
Klinefelter syndrome	1	View sentences
arrhythmia	1	View sentences
asthma	1	View sentences
autism spectrum disorder	1	View sentences
congenital cataract	1	View sentences
diabetes mellitus	1	View sentences
endometrial cancer	1	View sentences
familial hypercholesterolemia	1	View sentences
gastric cancer	1	View sentences
glycogen storage disease	1	View sentences
hepatocellular carcinoma	1	View sentences
hypertension	1	View sentences
infertility	1	View sentences
inflammatory bowel disease	1	View sentences
intellectual disability	1	View sentences
leukemia	1	View sentences
obesity	1	View sentences

and 5 more

Variants linked to BRAF through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

Variant	rsID	Articles	ClinVar
V600E	-	35	-
E586E	-	1	-
rs113488022	rs113488022	1	-

Regions or cities named in the abstracts of articles that mention BRAF.