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rs397507524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507524(-;-)
Make rs397507524(-;ACA)
Make rs397507524(ACA;ACA)
ReferenceGRCh38 38.1/141
Chromosome12
Position112472957
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507524
ebirs397507524
HLIrs397507524
Exacrs397507524
Varsomers397507524
Maprs397507524
PheGenIrs397507524
hapmaprs397507524
1000 genomesrs397507524
hgdprs397507524
ensemblrs397507524
gopubmedrs397507524
geneviewrs397507524
scholarrs397507524
googlers397507524
pharmgkbrs397507524
gwascentralrs397507524
openSNPrs397507524
23andMers397507524
23andMe allrs397507524
SNP Nexus

SNPshotrs397507524
SNPdbers397507524
MSV3drs397507524
GWAS Ctlgrs397507524
Max Magnitude0
ClinVar
Risk rs397507524(ACA;ACA)
Alt rs397507524(ACA;ACA)
Reference rs397507524(;)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene PTPN11
CLNDBN Rasopathy
Reversed 0
HGVS NC_000012.11:g.112910759_112910761dupACA
CLNSRC ClinVar
CLNACC RCV000033498.4,