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rs398123323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123323(-;-)
Make rs398123323(-;A)
Make rs398123323(A;A)
ReferenceGRCh38 38.1/141
Chromosome10
Position87933164
GenePTEN
is asnp
is mentioned by
dbSNPrs398123323
ebirs398123323
HLIrs398123323
Exacrs398123323
Varsomers398123323
Maprs398123323
PheGenIrs398123323
hapmaprs398123323
1000 genomesrs398123323
hgdprs398123323
ensemblrs398123323
gopubmedrs398123323
geneviewrs398123323
scholarrs398123323
googlers398123323
pharmgkbrs398123323
gwascentralrs398123323
openSNPrs398123323
23andMers398123323
23andMe allrs398123323
SNP Nexus

SNPshotrs398123323
SNPdbers398123323
MSV3drs398123323
GWAS Ctlgrs398123323
Max Magnitude0
ClinVar
Risk rs398123323(A;A)
Alt rs398123323(A;A)
Reference rs398123323(;)
Significance Pathogenic
Disease Macrocephaly/autism syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Macrocephaly/autism syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692921dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000032874.3, RCV000078617.3, RCV000162814.1,