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rs587776666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;ACAAT) 6.3 PTEN hamartoma tumor syndrome
(ACAAT;ACAAT) 0 common in clinvar


Make rs587776666(-;-)
ReferenceGRCh38 38.1/142
Chromosome10
Position87933106
GenePTEN
is asnp
is mentioned by
dbSNPrs587776666
dbSNP (old)rs587776666
ClinGenrs587776666
ebirs587776666
HLIrs587776666
Exacrs587776666
Gnomadrs587776666
Varsomers587776666
Maprs587776666
PheGenIrs587776666
Biobankrs587776666
1000 genomesrs587776666
hgdprs587776666
ensemblrs587776666
gopubmedrs587776666
geneviewrs587776666
scholarrs587776666
googlers587776666
pharmgkbrs587776666
gwascentralrs587776666
openSNPrs587776666
23andMers587776666
23andMe allrs587776666
SNP Nexus

SNPshotrs587776666
SNPdbers587776666
MSV3drs587776666
GWAS Ctlgrs587776666
Max Magnitude6.3
ClinVar
Risk rs587776666(-;-)
Alt rs587776666(-;-)
Reference Rs587776666(ACAAT;ACAAT)
Significance Pathogenic
Disease Cowden syndrome 1 PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1 PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692863_89692867delACAAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008262.2, RCV000460680.1,