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rs398123318

From SNPedia

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Geno Mag Summary
(GTAA;GTAA) 0 common in clinvar
Make rs398123318(-;-)
Make rs398123318(-;AGTA)
Make rs398123318(AGTA;AGTA)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925561
GenePTEN
is asnp
is mentioned by
dbSNPrs398123318
ebirs398123318
HLIrs398123318
Exacrs398123318
Varsomers398123318
Maprs398123318
PheGenIrs398123318
hapmaprs398123318
1000 genomesrs398123318
hgdprs398123318
ensemblrs398123318
gopubmedrs398123318
geneviewrs398123318
scholarrs398123318
googlers398123318
pharmgkbrs398123318
gwascentralrs398123318
openSNPrs398123318
23andMers398123318
23andMe allrs398123318
SNP Nexus

SNPshotrs398123318
SNPdbers398123318
MSV3drs398123318
GWAS Ctlgrs398123318
Max Magnitude0
ClinVar
Risk rs398123318(;)
Alt rs398123318(;)
Reference rs398123318(GTAA;GTAA)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89685318_89685321delAGTA
CLNSRC HGMD
CLNACC RCV000078609.3, RCV000217746.1,