rs121913336

Orientation

minus

Stabilized

minus

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

Make rs121913336(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753374

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913336
dbSNP (classic)	rs121913336
ClinGen	rs121913336
ebi	rs121913336
HLI	rs121913336
Exac	rs121913336
Gnomad	rs121913336
Varsome	rs121913336
LitVar	rs121913336
Map	rs121913336
PheGenI	rs121913336
Biobank	rs121913336
1000 genomes	rs121913336
hgdp	rs121913336
ensembl	rs121913336
geneview	rs121913336
scholar	rs121913336
google	rs121913336
pharmgkb	rs121913336
gwascentral	rs121913336
openSNP	rs121913336
23andMe	rs121913336
SNPshot	rs121913336
SNPdbe	rs121913336
MSV3d	rs121913336
GWAS Ctlg	rs121913336

Max Magnitude

0

ClinVar
Risk	Rs121913336(A;A) rs121913336(G;G)
Alt	Rs121913336(A;A) rs121913336(G;G)
Reference	Rs121913336(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	BRAF
CLNDBN	Neoplasm
Reversed	1
HGVS	NC_000007.13:g.140453174G>C; NC_000007.13:g.140453174G>T
CLNSRC
CLNACC	RCV000420521.1, RCV000431213.1,