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rs587781354

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587781354(-;-)
Make rs587781354(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87957990
GenePTEN
is asnp
is mentioned by
dbSNPrs587781354
ebirs587781354
HLIrs587781354
Exacrs587781354
Varsomers587781354
Maprs587781354
PheGenIrs587781354
hapmaprs587781354
1000 genomesrs587781354
hgdprs587781354
ensemblrs587781354
gopubmedrs587781354
geneviewrs587781354
scholarrs587781354
googlers587781354
pharmgkbrs587781354
gwascentralrs587781354
openSNPrs587781354
23andMers587781354
23andMe allrs587781354
SNP Nexus

SNPshotrs587781354
SNPdbers587781354
MSV3drs587781354
GWAS Ctlgrs587781354
Max Magnitude0
ClinVar
Risk rs587781354(;)
Alt rs587781354(;)
Reference rs587781354(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717747_89717748delTT
CLNSRC
CLNACC RCV000129138.2,