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

rs397507478

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507478(G;T)
Make rs397507478(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140777014
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507478
ebirs397507478
HLIrs397507478
Exacrs397507478
Varsomers397507478
Maprs397507478
PheGenIrs397507478
hapmaprs397507478
1000 genomesrs397507478
hgdprs397507478
ensemblrs397507478
gopubmedrs397507478
geneviewrs397507478
scholarrs397507478
googlers397507478
pharmgkbrs397507478
gwascentralrs397507478
openSNPrs397507478
23andMers397507478
23andMe allrs397507478
SNP Nexus

SNPshotrs397507478
SNPdbers397507478
MSV3drs397507478
GWAS Ctlgrs397507478
Max Magnitude0
ClinVar
Risk rs397507478(T;T)
Alt rs397507478(T;T)
Reference rs397507478(G;G)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140476814C>A
CLNSRC ClinVar
CLNACC RCV000033323.2,