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rs876661060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CA) 6.3 Hereditary cancer predisposing syndrome
(CA;CA) 0 common in clinvar


Make rs876661060(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933111
GenePTEN
is asnp
is mentioned by
dbSNPrs876661060
dbSNP (old)rs876661060
ClinGenrs876661060
ebirs876661060
HLIrs876661060
Exacrs876661060
Gnomadrs876661060
Varsomers876661060
Maprs876661060
PheGenIrs876661060
Biobankrs876661060
1000 genomesrs876661060
hgdprs876661060
ensemblrs876661060
gopubmedrs876661060
geneviewrs876661060
scholarrs876661060
googlers876661060
pharmgkbrs876661060
gwascentralrs876661060
openSNPrs876661060
23andMers876661060
23andMe allrs876661060
SNP Nexus

SNPshotrs876661060
SNPdbers876661060
MSV3drs876661060
GWAS Ctlgrs876661060
Max Magnitude6.3
ClinVar
Risk rs876661060(-;-)
Alt rs876661060(-;-)
Reference Rs876661060(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692868_89692869delCA
CLNSRC
CLNACC RCV000222845.1,