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rs869312776

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312776(G;G)
Make rs869312776(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933167
GenePTEN
is asnp
is mentioned by
dbSNPrs869312776
ebirs869312776
HLIrs869312776
Exacrs869312776
Varsomers869312776
Maprs869312776
PheGenIrs869312776
hapmaprs869312776
1000 genomesrs869312776
hgdprs869312776
ensemblrs869312776
gopubmedrs869312776
geneviewrs869312776
scholarrs869312776
googlers869312776
pharmgkbrs869312776
gwascentralrs869312776
openSNPrs869312776
23andMers869312776
23andMe allrs869312776
SNP Nexus

SNPshotrs869312776
SNPdbers869312776
MSV3drs869312776
GWAS Ctlgrs869312776
Max Magnitude0
ClinVar
Risk rs869312776(G;G)
Alt rs869312776(G;G)
Reference rs869312776(T;T)
Significance Probable-Pathogenic
Disease Cowden syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000010.10:g.89692924T>G
CLNSRC
CLNACC RCV000210082.1,