rs121913335

Orientation

minus

Stabilized

minus

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

Make rs121913335(A;C)

Make rs121913335(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753375

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913335
dbSNP (classic)	rs121913335
ClinGen	rs121913335
ebi	rs121913335
HLI	rs121913335
Exac	rs121913335
Gnomad	rs121913335
Varsome	rs121913335
LitVar	rs121913335
Map	rs121913335
PheGenI	rs121913335
Biobank	rs121913335
1000 genomes	rs121913335
hgdp	rs121913335
ensembl	rs121913335
geneview	rs121913335
scholar	rs121913335
google	rs121913335
pharmgkb	rs121913335
gwascentral	rs121913335
openSNP	rs121913335
23andMe	rs121913335
SNPshot	rs121913335
SNPdbe	rs121913335
MSV3d	rs121913335
GWAS Ctlg	rs121913335

Max Magnitude

0

ClinVar
Risk	rs121913335(C;C)
Alt	rs121913335(C;C)
Reference	Rs121913335(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	BRAF
CLNDBN	Neoplasm
Reversed	1
HGVS	NC_000007.13:g.140453175T>G
CLNSRC
CLNACC	RCV000434950.1,