rs121913351

Orientation

minus

Stabilized

minus

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

Make rs121913351(C;C)

Make rs121913351(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140781611

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913351
dbSNP (classic)	rs121913351
ClinGen	rs121913351
ebi	rs121913351
HLI	rs121913351
Exac	rs121913351
Gnomad	rs121913351
Varsome	rs121913351
LitVar	rs121913351
Map	rs121913351
PheGenI	rs121913351
Biobank	rs121913351
1000 genomes	rs121913351
hgdp	rs121913351
ensembl	rs121913351
geneview	rs121913351
scholar	rs121913351
google	rs121913351
pharmgkb	rs121913351
gwascentral	rs121913351
openSNP	rs121913351
23andMe	rs121913351
SNPshot	rs121913351
SNPdbe	rs121913351
MSV3d	rs121913351
GWAS Ctlg	rs121913351

Max Magnitude

0

OMIM	164757
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913351(A;A) rs121913351(C;C) rs121913351(T;T)
Alt	rs121913351(A;A) rs121913351(C;C) rs121913351(T;T)
Reference	Rs121913351(G;G)
Significance	Other
Disease	Adenocarcinoma of lung Non-small cell lung cancer Multiple myeloma Malignant melanoma of skin Colorectal Neoplasms Lung cancer Squamous cell carcinoma of the head and neck Squamous cell carcinoma of lung Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Adenocarcinoma of lung Non-small cell lung cancer Multiple myeloma Malignant melanoma of skin Colorectal Neoplasms Lung cancer Squamous cell carcinoma of the head and neck Squamous cell carcinoma of lung Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140481411C>A; NC_000007.13:g.140481411C>G; NC_000007.13:g.140481411C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015001.6, RCV000037916.3, RCV000421693.1, RCV000424032.1, RCV000429151.1, RCV000436576.1, RCV000438708.1, RCV000438953.1, RCV000418222.1, RCV000424689.1, RCV000427554.1, RCV000435402.1, RCV000438268.1, RCV000444041.1, RCV000444553.1, RCV000424079.1, RCV000427285.1, RCV000431475.1, RCV000434755.1, RCV000437081.1, RCV000442274.1, RCV000443232.1,