rs121913349

Orientation

minus

Stabilized

minus

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

Make rs121913349(C;C)

Make rs121913349(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

140781618

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913349
dbSNP (classic)	rs121913349
ClinGen	rs121913349
ebi	rs121913349
HLI	rs121913349
Exac	rs121913349
Gnomad	rs121913349
Varsome	rs121913349
LitVar	rs121913349
Map	rs121913349
PheGenI	rs121913349
Biobank	rs121913349
1000 genomes	rs121913349
hgdp	rs121913349
ensembl	rs121913349
geneview	rs121913349
scholar	rs121913349
google	rs121913349
pharmgkb	rs121913349
gwascentral	rs121913349
openSNP	rs121913349
23andMe	rs121913349
SNPshot	rs121913349
SNPdbe	rs121913349
MSV3d	rs121913349
GWAS Ctlg	rs121913349

Max Magnitude

0

ClinVar
Risk	rs121913349(A;A) rs121913349(C;C)
Alt	rs121913349(A;A) rs121913349(C;C)
Reference	Rs121913349(G;G)
Significance	Pathogenic
Disease	not provided Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	not provided Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140481418C>G; NC_000007.13:g.140481418C>T
CLNSRC
CLNACC	RCV000304268.1, RCV000413557.1, RCV000429423.1,