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rs397507551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507551(A;G)
Make rs397507551(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112489171
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507551
ebirs397507551
HLIrs397507551
Exacrs397507551
Varsomers397507551
Maprs397507551
PheGenIrs397507551
hapmaprs397507551
1000 genomesrs397507551
hgdprs397507551
ensemblrs397507551
gopubmedrs397507551
geneviewrs397507551
scholarrs397507551
googlers397507551
pharmgkbrs397507551
gwascentralrs397507551
openSNPrs397507551
23andMers397507551
23andMe allrs397507551
SNP Nexus

SNPshotrs397507551
SNPdbers397507551
MSV3drs397507551
GWAS Ctlgrs397507551
Max Magnitude0
ClinVar
Risk rs397507551(G;G)
Alt rs397507551(G;G)
Reference rs397507551(A;A)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene PTPN11
CLNDBN Rasopathy
Reversed 0
HGVS NC_000012.11:g.112926975A>G
CLNSRC ClinVar
CLNACC RCV000033556.2,