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rs587780006

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780006(-;-)
Make rs587780006(-;TT)
Make rs587780006(TT;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87960976
GenePTEN
is asnp
is mentioned by
dbSNPrs587780006
ebirs587780006
HLIrs587780006
Exacrs587780006
Varsomers587780006
Maprs587780006
PheGenIrs587780006
hapmaprs587780006
1000 genomesrs587780006
hgdprs587780006
ensemblrs587780006
gopubmedrs587780006
geneviewrs587780006
scholarrs587780006
googlers587780006
pharmgkbrs587780006
gwascentralrs587780006
openSNPrs587780006
23andMers587780006
23andMe allrs587780006
SNP Nexus

SNPshotrs587780006
SNPdbers587780006
MSV3drs587780006
GWAS Ctlgrs587780006
Max Magnitude0
ClinVar
Risk rs587780006(TT;TT)
Alt rs587780006(TT;TT)
Reference rs587780006(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720733_89720734insTT
CLNSRC
CLNACC RCV000115589.2,