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

rs180177037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177037(A;G)
Make rs180177037(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140778013
GeneBRAF
is asnp
is mentioned by
dbSNPrs180177037
ebirs180177037
HLIrs180177037
Exacrs180177037
Varsomers180177037
Maprs180177037
PheGenIrs180177037
hapmaprs180177037
1000 genomesrs180177037
hgdprs180177037
ensemblrs180177037
gopubmedrs180177037
geneviewrs180177037
scholarrs180177037
googlers180177037
pharmgkbrs180177037
gwascentralrs180177037
openSNPrs180177037
23andMers180177037
23andMe allrs180177037
SNP Nexus

SNPshotrs180177037
SNPdbers180177037
MSV3drs180177037
GWAS Ctlgrs180177037
Max Magnitude0
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
CLNACC RCV000015010.27, RCV000207517.2,