Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177033

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177033(G;G)
Make rs180177033(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140781620
GeneBRAF
is asnp
is mentioned by
dbSNPrs180177033
ebirs180177033
HLIrs180177033
Exacrs180177033
Varsomers180177033
Maprs180177033
PheGenIrs180177033
hapmaprs180177033
1000 genomesrs180177033
hgdprs180177033
ensemblrs180177033
gopubmedrs180177033
geneviewrs180177033
scholarrs180177033
googlers180177033
pharmgkbrs180177033
gwascentralrs180177033
openSNPrs180177033
23andMers180177033
23andMe allrs180177033
SNP Nexus

SNPshotrs180177033
SNPdbers180177033
MSV3drs180177033
GWAS Ctlgrs180177033
Max Magnitude0
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
CLNACC RCV000014996.6,