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rs869312777

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312777(C;G)
Make rs869312777(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933245
GenePTEN
is asnp
is mentioned by
dbSNPrs869312777
ebirs869312777
HLIrs869312777
Exacrs869312777
Varsomers869312777
Maprs869312777
PheGenIrs869312777
hapmaprs869312777
1000 genomesrs869312777
hgdprs869312777
ensemblrs869312777
gopubmedrs869312777
geneviewrs869312777
scholarrs869312777
googlers869312777
pharmgkbrs869312777
gwascentralrs869312777
openSNPrs869312777
23andMers869312777
23andMe allrs869312777
SNP Nexus

SNPshotrs869312777
SNPdbers869312777
MSV3drs869312777
GWAS Ctlgrs869312777
Max Magnitude0
ClinVar
Risk rs869312777(G;G)
Alt rs869312777(G;G)
Reference rs869312777(C;C)
Significance Probable-Pathogenic
Disease Cowden syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000010.10:g.89693002C>G
CLNSRC
CLNACC RCV000210132.1,