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rs398123316

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123316(A;T)
Make rs398123316(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87925530
GenePTEN
is asnp
is mentioned by
dbSNPrs398123316
ebirs398123316
HLIrs398123316
Exacrs398123316
Varsomers398123316
Maprs398123316
PheGenIrs398123316
hapmaprs398123316
1000 genomesrs398123316
hgdprs398123316
ensemblrs398123316
gopubmedrs398123316
geneviewrs398123316
scholarrs398123316
googlers398123316
pharmgkbrs398123316
gwascentralrs398123316
openSNPrs398123316
23andMers398123316
23andMe allrs398123316
SNP Nexus

SNPshotrs398123316
SNPdbers398123316
MSV3drs398123316
GWAS Ctlgrs398123316
Max Magnitude0
ClinVar
Risk rs398123316(G,T;G,T)
Alt rs398123316(G,T;G,T)
Reference rs398123316(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89685287A>G; NC_000010.10:g.89685287A>T
CLNSRC
CLNACC RCV000169791.1, RCV000078607.3,