rs121913375

Orientation

minus

Stabilized

minus

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

Make rs121913375(C;T)

Make rs121913375(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753339

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913375
dbSNP (classic)	rs121913375
ClinGen	rs121913375
ebi	rs121913375
HLI	rs121913375
Exac	rs121913375
Gnomad	rs121913375
Varsome	rs121913375
LitVar	rs121913375
Map	rs121913375
PheGenI	rs121913375
Biobank	rs121913375
1000 genomes	rs121913375
hgdp	rs121913375
ensembl	rs121913375
geneview	rs121913375
scholar	rs121913375
google	rs121913375
pharmgkb	rs121913375
gwascentral	rs121913375
openSNP	rs121913375
23andMe	rs121913375
SNPshot	rs121913375
SNPdbe	rs121913375
MSV3d	rs121913375
GWAS Ctlg	rs121913375

Max Magnitude

0

ClinVar
Risk	rs121913375(G;G) rs121913375(T;T)
Alt	rs121913375(G;G) rs121913375(T;T)
Reference	Rs121913375(C;C)
Significance	Pathogenic
Disease	not provided Malignant melanoma Neoplasm
Variation	info
Gene	BRAF
CLNDBN	not provided Malignant melanoma Neoplasm
Reversed	1
HGVS	NC_000007.13:g.140453139G>A; NC_000007.13:g.140453139G>C
CLNSRC	ClinVar
CLNACC	RCV000033334.4, RCV000433036.1, RCV000440873.1, RCV000291177.1,