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rs587776669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776669(-;-)
Make rs587776669(-;A)
ReferenceGRCh38 38.1/142
Chromosome10
Position87957914
GenePTEN
is asnp
is mentioned by
dbSNPrs587776669
ebirs587776669
HLIrs587776669
Exacrs587776669
Varsomers587776669
Maprs587776669
PheGenIrs587776669
hapmaprs587776669
1000 genomesrs587776669
hgdprs587776669
ensemblrs587776669
gopubmedrs587776669
geneviewrs587776669
scholarrs587776669
googlers587776669
pharmgkbrs587776669
gwascentralrs587776669
openSNPrs587776669
23andMers587776669
23andMe allrs587776669
SNP Nexus

SNPshotrs587776669
SNPdbers587776669
MSV3drs587776669
GWAS Ctlgrs587776669
Max Magnitude0
ClinVar
Risk rs587776669(;)
Alt rs587776669(;)
Reference rs587776669(A;A)
Significance Pathogenic
Disease Cowden syndrome 1
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1
Reversed 0
HGVS NC_000010.10:g.89717671delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008268.2,