rs121913376

Orientation

minus

Stabilized

minus

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

Make rs121913376(G;T)

Make rs121913376(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140781597

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913376
dbSNP (classic)	rs121913376
ClinGen	rs121913376
ebi	rs121913376
HLI	rs121913376
Exac	rs121913376
Gnomad	rs121913376
Varsome	rs121913376
LitVar	rs121913376
Map	rs121913376
PheGenI	rs121913376
Biobank	rs121913376
1000 genomes	rs121913376
hgdp	rs121913376
ensembl	rs121913376
geneview	rs121913376
scholar	rs121913376
google	rs121913376
pharmgkb	rs121913376
gwascentral	rs121913376
openSNP	rs121913376
23andMe	rs121913376
SNPshot	rs121913376
SNPdbe	rs121913376
MSV3d	rs121913376
GWAS Ctlg	rs121913376

Max Magnitude

0

ClinVar
Risk	rs121913376(A;A) rs121913376(T;T)
Alt	rs121913376(A;A) rs121913376(T;T)
Reference	Rs121913376(G;G)
Significance	Probable-Pathogenic
Disease	not provided Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	not provided Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140481397C>A; NC_000007.13:g.140481397C>T
CLNSRC	ClinVar
CLNACC	RCV000033308.5, RCV000417719.1, RCV000033309.4,