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rs587776670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776670(-;-)
Make rs587776670(-;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position87952211
GenePTEN
is asnp
is mentioned by
dbSNPrs587776670
ebirs587776670
HLIrs587776670
Exacrs587776670
Varsomers587776670
Maprs587776670
PheGenIrs587776670
hapmaprs587776670
1000 genomesrs587776670
hgdprs587776670
ensemblrs587776670
gopubmedrs587776670
geneviewrs587776670
scholarrs587776670
googlers587776670
pharmgkbrs587776670
gwascentralrs587776670
openSNPrs587776670
23andMers587776670
23andMe allrs587776670
SNP Nexus

SNPshotrs587776670
SNPdbers587776670
MSV3drs587776670
GWAS Ctlgrs587776670
Max Magnitude0
ClinVar
Risk rs587776670(;)
Alt rs587776670(;)
Reference rs587776670(C;C)
Significance Pathogenic
Disease Bannayan-Riley-Ruvalcaba syndrome
Variation info
Gene PTEN
CLNDBN Bannayan-Riley-Ruvalcaba syndrome
Reversed 0
HGVS NC_000010.10:g.89711968delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000008269.3,