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rs180177032

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177032(G;T)
Make rs180177032(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140781623
GeneBRAF
is asnp
is mentioned by
dbSNPrs180177032
ebirs180177032
HLIrs180177032
Exacrs180177032
Varsomers180177032
Maprs180177032
PheGenIrs180177032
hapmaprs180177032
1000 genomesrs180177032
hgdprs180177032
ensemblrs180177032
gopubmedrs180177032
geneviewrs180177032
scholarrs180177032
googlers180177032
pharmgkbrs180177032
gwascentralrs180177032
openSNPrs180177032
23andMers180177032
23andMe allrs180177032
SNP Nexus

SNPshotrs180177032
SNPdbers180177032
MSV3drs180177032
GWAS Ctlgrs180177032
Max Magnitude0
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
CLNACC RCV000014995.6,