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rs397516811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516811(A;A)
Make rs397516811(A;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position112477655
GenePTPN11
is asnp
is mentioned by
dbSNPrs397516811
ebirs397516811
HLIrs397516811
Exacrs397516811
Varsomers397516811
Maprs397516811
PheGenIrs397516811
hapmaprs397516811
1000 genomesrs397516811
hgdprs397516811
ensemblrs397516811
gopubmedrs397516811
geneviewrs397516811
scholarrs397516811
googlers397516811
pharmgkbrs397516811
gwascentralrs397516811
openSNPrs397516811
23andMers397516811
23andMe allrs397516811
SNP Nexus

SNPshotrs397516811
SNPdbers397516811
MSV3drs397516811
GWAS Ctlgrs397516811
Max Magnitude0
ClinVar
Risk rs397516811(A;A)
Alt rs397516811(A;A)
Reference rs397516811(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene PTPN11
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.112915459T>A
CLNSRC ClinVar
CLNACC RCV000037666.3,