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rs587782341

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782341(-;-)
Make rs587782341(-;A)
Make rs587782341(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87957959
GenePTEN
is asnp
is mentioned by
dbSNPrs587782341
ebirs587782341
HLIrs587782341
Exacrs587782341
Varsomers587782341
Maprs587782341
PheGenIrs587782341
hapmaprs587782341
1000 genomesrs587782341
hgdprs587782341
ensemblrs587782341
gopubmedrs587782341
geneviewrs587782341
scholarrs587782341
googlers587782341
pharmgkbrs587782341
gwascentralrs587782341
openSNPrs587782341
23andMers587782341
23andMe allrs587782341
SNP Nexus

SNPshotrs587782341
SNPdbers587782341
MSV3drs587782341
GWAS Ctlgrs587782341
Max Magnitude0
ClinVar
Risk rs587782341(A;A)
Alt rs587782341(A;A)
Reference rs587782341(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717716dupA
CLNSRC
CLNACC RCV000131274.2,