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rs869025607

From SNPedia

Orientationminus
Geno Mag Summary
(ACA;ACA) 0 common in clinvar
Make rs869025607(-;-)
Make rs869025607(-;ACA)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position140781598
GeneBRAF
is asnp
is mentioned by
dbSNPrs869025607
ebirs869025607
HLIrs869025607
Exacrs869025607
Varsomers869025607
Maprs869025607
PheGenIrs869025607
hapmaprs869025607
1000 genomesrs869025607
hgdprs869025607
ensemblrs869025607
gopubmedrs869025607
geneviewrs869025607
scholarrs869025607
googlers869025607
pharmgkbrs869025607
gwascentralrs869025607
openSNPrs869025607
23andMers869025607
23andMe allrs869025607
SNP Nexus

SNPshotrs869025607
SNPdbers869025607
MSV3drs869025607
GWAS Ctlgrs869025607
Max Magnitude0
ClinVar
Risk rs869025607(;)
Alt rs869025607(;)
Reference rs869025607(ACA;ACA)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140481398_140481400delTGT
CLNSRC
CLNACC RCV000208751.1,