rs121913364

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs121913364(A;G)

Make rs121913364(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753334

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913364
dbSNP (classic)	rs121913364
ClinGen	rs121913364
ebi	rs121913364
HLI	rs121913364
Exac	rs121913364
Gnomad	rs121913364
Varsome	rs121913364
LitVar	rs121913364
Map	rs121913364
PheGenI	rs121913364
Biobank	rs121913364
1000 genomes	rs121913364
hgdp	rs121913364
ensembl	rs121913364
geneview	rs121913364
scholar	rs121913364
google	rs121913364
pharmgkb	rs121913364
gwascentral	rs121913364
openSNP	rs121913364
23andMe	rs121913364
SNPshot	rs121913364
SNPdbe	rs121913364
MSV3d	rs121913364
GWAS Ctlg	rs121913364

Max Magnitude

0

OMIM	164757
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121913364(C;C) rs121913364(G;G)
Alt	rs121913364(C;C) rs121913364(G;G)
Reference	Rs121913364(A;A)
Significance	Pathogenic
Disease	Carcinoma of colon Thyroid cancer Non-small cell lung cancer Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Neoplasm of the thyroid gland Adenocarcinoma of prostate Adenocarcinoma of lung Chronic lymphocytic leukemia Malignant melanoma Neoplasm not provided Rasopathy
Variation	info
Gene	BRAF
CLNDBN	Carcinoma of colon Thyroid cancer, follicular Non-small cell lung cancer Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Neoplasm of the thyroid gland Adenocarcinoma of prostate Adenocarcinoma of lung Chronic lymphocytic leukemia Malignant melanoma Neoplasm not provided Rasopathy
Reversed	1
HGVS	NC_000007.13:g.140453134T>C; NC_000007.13:g.140453134T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein) HGMD
CLNACC	RCV000014999.7, RCV000015000.7, RCV000037938.2, RCV000422559.1, RCV000423181.1, RCV000425399.1, RCV000432202.1, RCV000432849.1, RCV000433498.1, RCV000440232.1, RCV000440872.1, RCV000443528.1, RCV000034332.6, RCV000150201.2,