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rs397507484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507484(A;T)
Make rs397507484(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753333
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507484
ebirs397507484
HLIrs397507484
Exacrs397507484
Varsomers397507484
Maprs397507484
PheGenIrs397507484
hapmaprs397507484
1000 genomesrs397507484
hgdprs397507484
ensemblrs397507484
gopubmedrs397507484
geneviewrs397507484
scholarrs397507484
googlers397507484
pharmgkbrs397507484
gwascentralrs397507484
openSNPrs397507484
23andMers397507484
23andMe allrs397507484
SNP Nexus

SNPshotrs397507484
SNPdbers397507484
MSV3drs397507484
GWAS Ctlgrs397507484
Max Magnitude0
ClinVar
Risk rs397507484(C,T;C,T)
Alt rs397507484(C,T;C,T)
Reference rs397507484(A;A)
Significance Other
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140453133T>A; NC_000007.13:g.140453133T>G
CLNSRC ClinVar
CLNACC RCV000033336.4, RCV000037939.3,