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rs397507521

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507521(A;A)
Make rs397507521(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112453317
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507521
ebirs397507521
HLIrs397507521
Exacrs397507521
Varsomers397507521
Maprs397507521
PheGenIrs397507521
hapmaprs397507521
1000 genomesrs397507521
hgdprs397507521
ensemblrs397507521
gopubmedrs397507521
geneviewrs397507521
scholarrs397507521
googlers397507521
pharmgkbrs397507521
gwascentralrs397507521
openSNPrs397507521
23andMers397507521
23andMe allrs397507521
SNP Nexus

SNPshotrs397507521
SNPdbers397507521
MSV3drs397507521
GWAS Ctlgrs397507521
Max Magnitude0
ClinVar
Risk rs397507521(A;A)
Alt rs397507521(A;A)
Reference rs397507521(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene PTPN11
CLNDBN not provided not specified
Reversed 0
HGVS NC_000012.11:g.112891121G>A
CLNSRC ClinVar
CLNACC RCV000033492.4, RCV000121913.1,