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

rs397516905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516905(C;C)
Make rs397516905(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801479
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516905
ebirs397516905
HLIrs397516905
Exacrs397516905
Varsomers397516905
Maprs397516905
PheGenIrs397516905
hapmaprs397516905
1000 genomesrs397516905
hgdprs397516905
ensemblrs397516905
gopubmedrs397516905
geneviewrs397516905
scholarrs397516905
googlers397516905
pharmgkbrs397516905
gwascentralrs397516905
openSNPrs397516905
23andMers397516905
23andMe allrs397516905
SNP Nexus

SNPshotrs397516905
SNPdbers397516905
MSV3drs397516905
GWAS Ctlgrs397516905
Max Magnitude0
ClinVar
Risk rs397516905(C;C)
Alt rs397516905(C;C)
Reference rs397516905(G;G)
Significance Probable-Pathogenic
Disease Noonan syndrome
Variation info
Gene BRAF
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000007.13:g.140501279C>G
CLNSRC ClinVar
CLNACC RCV000037962.3,