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rs397509344

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509344(C;G)
Make rs397509344(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112488445
GenePTPN11
is asnp
is mentioned by
dbSNPrs397509344
ebirs397509344
HLIrs397509344
Exacrs397509344
Varsomers397509344
Maprs397509344
PheGenIrs397509344
hapmaprs397509344
1000 genomesrs397509344
hgdprs397509344
ensemblrs397509344
gopubmedrs397509344
geneviewrs397509344
scholarrs397509344
googlers397509344
pharmgkbrs397509344
gwascentralrs397509344
openSNPrs397509344
23andMers397509344
23andMe allrs397509344
SNP Nexus

SNPshotrs397509344
SNPdbers397509344
MSV3drs397509344
GWAS Ctlgrs397509344
Max Magnitude0
ClinVar
Risk rs397509344(G;G)
Alt rs397509344(G;G)
Reference rs397509344(C;C)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene PTPN11
CLNDBN Rasopathy
Reversed 0
HGVS NC_000012.11:g.112926249C>G
CLNSRC ClinVar
CLNACC RCV000049229.1,