rs397516905

Orientation

minus

Stabilized

minus

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

Make rs397516905(C;C)

Make rs397516905(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140801479

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs397516905
dbSNP (classic)	rs397516905
ClinGen	rs397516905
ebi	rs397516905
HLI	rs397516905
Exac	rs397516905
Gnomad	rs397516905
Varsome	rs397516905
LitVar	rs397516905
Map	rs397516905
PheGenI	rs397516905
Biobank	rs397516905
1000 genomes	rs397516905
hgdp	rs397516905
ensembl	rs397516905
geneview	rs397516905
scholar	rs397516905
google	rs397516905
pharmgkb	rs397516905
gwascentral	rs397516905
openSNP	rs397516905
23andMe	rs397516905
SNPshot	rs397516905
SNPdbe	rs397516905
MSV3d	rs397516905
GWAS Ctlg	rs397516905

Max Magnitude

0

ClinVar
Risk	rs397516905(C;C)
Alt	rs397516905(C;C)
Reference	Rs397516905(G;G)
Significance	Probable-Pathogenic
Disease	Noonan syndrome
Variation	info
Gene	BRAF
CLNDBN	Noonan syndrome
Reversed	1
HGVS	NC_000007.13:g.140501279C>G
CLNSRC	ClinVar
CLNACC	RCV000037962.3,