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rs397507538

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507538(G;T)
Make rs397507538(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position112489029
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507538
ebirs397507538
HLIrs397507538
Exacrs397507538
Varsomers397507538
Maprs397507538
PheGenIrs397507538
hapmaprs397507538
1000 genomesrs397507538
hgdprs397507538
ensemblrs397507538
gopubmedrs397507538
geneviewrs397507538
scholarrs397507538
googlers397507538
pharmgkbrs397507538
gwascentralrs397507538
openSNPrs397507538
23andMers397507538
23andMe allrs397507538
SNP Nexus

SNPshotrs397507538
SNPdbers397507538
MSV3drs397507538
GWAS Ctlgrs397507538
Max Magnitude0
ClinVar
Risk rs397507538(T;T)
Alt rs397507538(T;T)
Reference rs397507538(G;G)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene PTPN11
CLNDBN Rasopathy
Reversed 0
HGVS NC_000012.11:g.112926833G>T
CLNSRC ClinVar
CLNACC RCV000033534.2,