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rs397507507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507507(A;A)
Make rs397507507(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112450358
GenePTPN11
is asnp
is mentioned by
dbSNPrs397507507
ebirs397507507
HLIrs397507507
Exacrs397507507
Varsomers397507507
Maprs397507507
PheGenIrs397507507
hapmaprs397507507
1000 genomesrs397507507
hgdprs397507507
ensemblrs397507507
gopubmedrs397507507
geneviewrs397507507
scholarrs397507507
googlers397507507
pharmgkbrs397507507
gwascentralrs397507507
openSNPrs397507507
23andMers397507507
23andMe allrs397507507
SNP Nexus

SNPshotrs397507507
SNPdbers397507507
MSV3drs397507507
GWAS Ctlgrs397507507
Max Magnitude0
ClinVar
Risk rs397507507(A,T;A,T)
Alt rs397507507(A,T;A,T)
Reference rs397507507(G;G)
Significance Other
Disease Noonan syndrome not provided
Variation info
Gene PTPN11
CLNDBN Noonan syndrome not provided
Reversed 0
HGVS NC_000012.11:g.112888162G>A; NC_000012.11:g.112888162G>T
CLNSRC HGMD
CLNACC RCV000151684.1, RCV000157700.2, RCV000034327.6,