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rs397507503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507503(C;T)
Make rs397507503(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position112450335
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507503
ebirs397507503
HLIrs397507503
Exacrs397507503
Varsomers397507503
Maprs397507503
PheGenIrs397507503
hapmaprs397507503
1000 genomesrs397507503
hgdprs397507503
ensemblrs397507503
gopubmedrs397507503
geneviewrs397507503
scholarrs397507503
googlers397507503
pharmgkbrs397507503
gwascentralrs397507503
openSNPrs397507503
23andMers397507503
23andMe allrs397507503
SNP Nexus

SNPshotrs397507503
SNPdbers397507503
MSV3drs397507503
GWAS Ctlgrs397507503
Max Magnitude0
ClinVar
Risk rs397507503(T;T)
Alt rs397507503(T;T)
Reference rs397507503(C;C)
Significance Probable-Pathogenic
Disease not provided Noonan syndrome
Variation info
Gene PTPN11
CLNDBN not provided Noonan syndrome
Reversed 0
HGVS NC_000012.11:g.112888139C>T
CLNSRC ClinVar
CLNACC RCV000033452.5, RCV000037621.3,