rs397507476

Orientation

minus

Stabilized

minus

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

Make rs397507476(A;C)

Make rs397507476(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140778011

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs397507476
dbSNP (classic)	rs397507476
ClinGen	rs397507476
ebi	rs397507476
HLI	rs397507476
Exac	rs397507476
Gnomad	rs397507476
Varsome	rs397507476
LitVar	rs397507476
Map	rs397507476
PheGenI	rs397507476
Biobank	rs397507476
1000 genomes	rs397507476
hgdp	rs397507476
ensembl	rs397507476
geneview	rs397507476
scholar	rs397507476
google	rs397507476
pharmgkb	rs397507476
gwascentral	rs397507476
openSNP	rs397507476
23andMe	rs397507476
SNPshot	rs397507476
SNPdbe	rs397507476
MSV3d	rs397507476
GWAS Ctlg	rs397507476

Max Magnitude

0

ClinVar
Risk	rs397507476(C;C) rs397507476(T;T)
Alt	rs397507476(C;C) rs397507476(T;T)
Reference	Rs397507476(A;A)
Significance	Other
Disease	not provided
Variation	info
Gene	BRAF
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.140477811T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000207509.2,