rs121913362

Orientation

minus

Stabilized

minus

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

Make rs121913362(A;G)

Make rs121913362(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753359

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913362
dbSNP (classic)	rs121913362
ClinGen	rs121913362
ebi	rs121913362
HLI	rs121913362
Exac	rs121913362
Gnomad	rs121913362
Varsome	rs121913362
LitVar	rs121913362
Map	rs121913362
PheGenI	rs121913362
Biobank	rs121913362
1000 genomes	rs121913362
hgdp	rs121913362
ensembl	rs121913362
geneview	rs121913362
scholar	rs121913362
google	rs121913362
pharmgkb	rs121913362
gwascentral	rs121913362
openSNP	rs121913362
23andMe	rs121913362
SNPshot	rs121913362
SNPdbe	rs121913362
MSV3d	rs121913362
GWAS Ctlg	rs121913362

Max Magnitude

0

ClinVar
Risk	rs121913362(G;G)
Alt	rs121913362(G;G)
Reference	Rs121913362(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	BRAF
CLNDBN	Neoplasm
Reversed	1
HGVS	NC_000007.13:g.140453159T>C
CLNSRC
CLNACC	RCV000437742.1,