rs180177037

Orientation

minus

Stabilized

minus

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

Make rs180177037(A;G)

Make rs180177037(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140778013

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs180177037
dbSNP (classic)	rs180177037
ClinGen	rs180177037
ebi	rs180177037
HLI	rs180177037
Exac	rs180177037
Gnomad	rs180177037
Varsome	rs180177037
LitVar	rs180177037
Map	rs180177037
PheGenI	rs180177037
Biobank	rs180177037
1000 genomes	rs180177037
hgdp	rs180177037
ensembl	rs180177037
geneview	rs180177037
scholar	rs180177037
google	rs180177037
pharmgkb	rs180177037
gwascentral	rs180177037
openSNP	rs180177037
23andMe	rs180177037
SNPshot	rs180177037
SNPdbe	rs180177037
MSV3d	rs180177037
GWAS Ctlg	rs180177037

Max Magnitude

0

ClinVar
Risk	rs180177037(G;G)
Alt	rs180177037(G;G)
Reference	Rs180177037(A;A)
Significance	Other
Disease	Cardiofaciocutaneous syndrome 1 not provided
Variation	info
Gene	BRAF
CLNDBN	Cardiofaciocutaneous syndrome 1 not provided
Reversed	1
HGVS	NC_000007.13:g.140477813T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015010.27, RCV000207517.2,