Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507537(A;C)
Make rs397507537(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position112488465
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507537
ebirs397507537
HLIrs397507537
Exacrs397507537
Varsomers397507537
Maprs397507537
PheGenIrs397507537
hapmaprs397507537
1000 genomesrs397507537
hgdprs397507537
ensemblrs397507537
gopubmedrs397507537
geneviewrs397507537
scholarrs397507537
googlers397507537
pharmgkbrs397507537
gwascentralrs397507537
openSNPrs397507537
23andMers397507537
23andMe allrs397507537
SNP Nexus

SNPshotrs397507537
SNPdbers397507537
MSV3drs397507537
GWAS Ctlgrs397507537
Max Magnitude0
ClinVar
Risk rs397507537(C;C)
Alt rs397507537(C;C)
Reference rs397507537(A;A)
Significance Pathogenic
Disease not provided Rasopathy
Variation info
Gene PTPN11
CLNDBN not provided Rasopathy
Reversed 0
HGVS NC_000012.11:g.112926269A>C
CLNSRC ClinVar
CLNACC RCV000033532.5, RCV000231162.1,