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rs397507513

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507513(A;C)
Make rs397507513(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position112450397
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507513
ebirs397507513
HLIrs397507513
Exacrs397507513
Varsomers397507513
Maprs397507513
PheGenIrs397507513
hapmaprs397507513
1000 genomesrs397507513
hgdprs397507513
ensemblrs397507513
gopubmedrs397507513
geneviewrs397507513
scholarrs397507513
googlers397507513
pharmgkbrs397507513
gwascentralrs397507513
openSNPrs397507513
23andMers397507513
23andMe allrs397507513
SNP Nexus

SNPshotrs397507513
SNPdbers397507513
MSV3drs397507513
GWAS Ctlgrs397507513
Max Magnitude0
ClinVar
Risk rs397507513(C;C)
Alt rs397507513(C;C)
Reference rs397507513(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112888201A>C
CLNSRC ClinVar
CLNACC RCV000033474.4,