rs180177033

Orientation

minus

Stabilized

minus

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

Make rs180177033(G;G)

Make rs180177033(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

140781620

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs180177033
dbSNP (classic)	rs180177033
ClinGen	rs180177033
ebi	rs180177033
HLI	rs180177033
Exac	rs180177033
Gnomad	rs180177033
Varsome	rs180177033
LitVar	rs180177033
Map	rs180177033
PheGenI	rs180177033
Biobank	rs180177033
1000 genomes	rs180177033
hgdp	rs180177033
ensembl	rs180177033
geneview	rs180177033
scholar	rs180177033
google	rs180177033
pharmgkb	rs180177033
gwascentral	rs180177033
openSNP	rs180177033
23andMe	rs180177033
SNPshot	rs180177033
SNPdbe	rs180177033
MSV3d	rs180177033
GWAS Ctlg	rs180177033

Max Magnitude

0

ClinVar
Risk	rs180177033(G;G)
Alt	rs180177033(G;G)
Reference	Rs180177033(T;T)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	BRAF
CLNDBN	Carcinoma of colon
Reversed	1
HGVS	NC_000007.13:g.140481420A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014996.6,