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rs397516825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516825(A;G)
Make rs397516825(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12604204
GeneRAF1
is asnp
is mentioned by
dbSNPrs397516825
ebirs397516825
HLIrs397516825
Exacrs397516825
Varsomers397516825
Maprs397516825
PheGenIrs397516825
hapmaprs397516825
1000 genomesrs397516825
hgdprs397516825
ensemblrs397516825
gopubmedrs397516825
geneviewrs397516825
scholarrs397516825
googlers397516825
pharmgkbrs397516825
gwascentralrs397516825
openSNPrs397516825
23andMers397516825
23andMe allrs397516825
SNP Nexus

SNPshotrs397516825
SNPdbers397516825
MSV3drs397516825
GWAS Ctlgrs397516825
Max Magnitude0
ClinVar
Risk rs397516825(G;G)
Alt rs397516825(G;G)
Reference rs397516825(A;A)
Significance Probable-Pathogenic
Disease Noonan syndrome
Variation info
Gene RAF1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000003.11:g.12645703T>C
CLNSRC ClinVar
CLNACC RCV000037699.2,