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rs397507475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507475(C;C)
Make rs397507475(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140778054
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507475
ClinGenrs397507475
ebirs397507475
HLIrs397507475
Exacrs397507475
Varsomers397507475
Maprs397507475
PheGenIrs397507475
hapmaprs397507475
1000 genomesrs397507475
hgdprs397507475
ensemblrs397507475
gopubmedrs397507475
geneviewrs397507475
scholarrs397507475
googlers397507475
pharmgkbrs397507475
gwascentralrs397507475
openSNPrs397507475
23andMers397507475
23andMe allrs397507475
SNP Nexus

SNPshotrs397507475
SNPdbers397507475
MSV3drs397507475
GWAS Ctlgrs397507475
Max Magnitude0
ClinVar
Risk rs397507475(C;C)
Alt rs397507475(C;C)
Reference Rs397507475(T;T)
Significance Pathogenic
Disease not provided Cardio-facio-cutaneous syndrome
Variation info
Gene BRAF
CLNDBN not provided Cardio-facio-cutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140477854A>G
CLNSRC ClinVar
CLNACC RCV000033311.4, RCV000150207.1,