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rs397507523

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507523(A;G)
Make rs397507523(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112472954
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507523
ebirs397507523
HLIrs397507523
Exacrs397507523
Varsomers397507523
Maprs397507523
PheGenIrs397507523
hapmaprs397507523
1000 genomesrs397507523
hgdprs397507523
ensemblrs397507523
gopubmedrs397507523
geneviewrs397507523
scholarrs397507523
googlers397507523
pharmgkbrs397507523
gwascentralrs397507523
openSNPrs397507523
23andMers397507523
23andMe allrs397507523
SNP Nexus

SNPshotrs397507523
SNPdbers397507523
MSV3drs397507523
GWAS Ctlgrs397507523
Max Magnitude0
ClinVar
Risk rs397507523(G;G)
Alt rs397507523(G;G)
Reference rs397507523(A;A)
Significance Other
Disease Rasopathy not provided
Variation info
Gene PTPN11
CLNDBN Rasopathy not provided
Reversed 0
HGVS NC_000012.11:g.112910758A>G
CLNSRC ClinVar
CLNACC RCV000033497.6, RCV000157681.1,