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rs398123315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123315(-;-)
Make rs398123315(-;A)
Make rs398123315(A;A)
ReferenceGRCh38 38.1/141
Chromosome10
Position87965300
GenePTEN
is asnp
is mentioned by
dbSNPrs398123315
ebirs398123315
HLIrs398123315
Exacrs398123315
Varsomers398123315
Maprs398123315
PheGenIrs398123315
hapmaprs398123315
1000 genomesrs398123315
hgdprs398123315
ensemblrs398123315
gopubmedrs398123315
geneviewrs398123315
scholarrs398123315
googlers398123315
pharmgkbrs398123315
gwascentralrs398123315
openSNPrs398123315
23andMers398123315
23andMe allrs398123315
SNP Nexus

SNPshotrs398123315
SNPdbers398123315
MSV3drs398123315
GWAS Ctlgrs398123315
Max Magnitude0
ClinVar
Risk rs398123315(A;A)
Alt rs398123315(A;A)
Reference rs398123315(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89725057_89725058insA
CLNSRC ClinVar
CLNACC RCV000078605.3,