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rs397507536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507536(A;A)
Make rs397507536(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112486532
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507536
ebirs397507536
HLIrs397507536
Exacrs397507536
Varsomers397507536
Maprs397507536
PheGenIrs397507536
hapmaprs397507536
1000 genomesrs397507536
hgdprs397507536
ensemblrs397507536
gopubmedrs397507536
geneviewrs397507536
scholarrs397507536
googlers397507536
pharmgkbrs397507536
gwascentralrs397507536
openSNPrs397507536
23andMers397507536
23andMe allrs397507536
SNP Nexus

SNPshotrs397507536
SNPdbers397507536
MSV3drs397507536
GWAS Ctlgrs397507536
Max Magnitude0
ClinVar
Risk rs397507536(A;A)
Alt rs397507536(A;A)
Reference rs397507536(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112924336G>A
CLNSRC ClinVar
CLNACC RCV000033528.4,