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rs397509345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397509345(AG;CC)
Make rs397509345(CC;CC)
ReferenceGRCh38 38.1/141
Chromosome12
Position112489093
GenePTPN11
is asnp
is mentioned by
dbSNPrs397509345
ebirs397509345
HLIrs397509345
Exacrs397509345
Varsomers397509345
Maprs397509345
PheGenIrs397509345
hapmaprs397509345
1000 genomesrs397509345
hgdprs397509345
ensemblrs397509345
gopubmedrs397509345
geneviewrs397509345
scholarrs397509345
googlers397509345
pharmgkbrs397509345
gwascentralrs397509345
openSNPrs397509345
23andMers397509345
23andMe allrs397509345
SNP Nexus

SNPshotrs397509345
SNPdbers397509345
MSV3drs397509345
GWAS Ctlgrs397509345
Max Magnitude0
ClinVar
Risk rs397509345(CC;CC)
Alt rs397509345(CC;CC)
Reference rs397509345(AG;AG)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene PTPN11
CLNDBN Rasopathy
Reversed 0
HGVS NC_000012.11:g.112926897_112926898delAGinsCC
CLNSRC ClinVar
CLNACC RCV000049230.1,