rs180177032

Orientation

minus

Stabilized

minus

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

Make rs180177032(G;T)

Make rs180177032(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

140781623

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs180177032
dbSNP (classic)	rs180177032
ClinGen	rs180177032
ebi	rs180177032
HLI	rs180177032
Exac	rs180177032
Gnomad	rs180177032
Varsome	rs180177032
LitVar	rs180177032
Map	rs180177032
PheGenI	rs180177032
Biobank	rs180177032
1000 genomes	rs180177032
hgdp	rs180177032
ensembl	rs180177032
geneview	rs180177032
scholar	rs180177032
google	rs180177032
pharmgkb	rs180177032
gwascentral	rs180177032
openSNP	rs180177032
23andMe	rs180177032
SNPshot	rs180177032
SNPdbe	rs180177032
MSV3d	rs180177032
GWAS Ctlg	rs180177032

Max Magnitude

0

ClinVar
Risk	rs180177032(T;T)
Alt	rs180177032(T;T)
Reference	Rs180177032(G;G)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	BRAF
CLNDBN	Carcinoma of colon
Reversed	1
HGVS	NC_000007.13:g.140481423C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014995.6,