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rs587781784

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781784(A;G)
Make rs587781784(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952116
GenePTEN
is asnp
is mentioned by
dbSNPrs587781784
ebirs587781784
HLIrs587781784
Exacrs587781784
Varsomers587781784
Maprs587781784
PheGenIrs587781784
hapmaprs587781784
1000 genomesrs587781784
hgdprs587781784
ensemblrs587781784
gopubmedrs587781784
geneviewrs587781784
scholarrs587781784
googlers587781784
pharmgkbrs587781784
gwascentralrs587781784
openSNPrs587781784
23andMers587781784
23andMe allrs587781784
SNP Nexus

SNPshotrs587781784
SNPdbers587781784
MSV3drs587781784
GWAS Ctlgrs587781784
Max Magnitude0
ClinVar
Risk rs587781784(G;G)
Alt rs587781784(G;G)
Reference rs587781784(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711873A>G
CLNSRC
CLNACC RCV000130038.3,