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rs397507519

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507519(A;C)
Make rs397507519(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position112450509
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507519
ebirs397507519
HLIrs397507519
Exacrs397507519
Varsomers397507519
Maprs397507519
PheGenIrs397507519
hapmaprs397507519
1000 genomesrs397507519
hgdprs397507519
ensemblrs397507519
gopubmedrs397507519
geneviewrs397507519
scholarrs397507519
googlers397507519
pharmgkbrs397507519
gwascentralrs397507519
openSNPrs397507519
23andMers397507519
23andMe allrs397507519
SNP Nexus

SNPshotrs397507519
SNPdbers397507519
MSV3drs397507519
GWAS Ctlgrs397507519
Max Magnitude0
ClinVar
Risk rs397507519(C;C)
Alt rs397507519(C;C)
Reference rs397507519(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112888313A>C
CLNSRC ClinVar
CLNACC RCV000033485.5,