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rs869312775

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312775(A;G)
Make rs869312775(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933103
GenePTEN
is asnp
is mentioned by
dbSNPrs869312775
ebirs869312775
HLIrs869312775
Exacrs869312775
Varsomers869312775
Maprs869312775
PheGenIrs869312775
hapmaprs869312775
1000 genomesrs869312775
hgdprs869312775
ensemblrs869312775
gopubmedrs869312775
geneviewrs869312775
scholarrs869312775
googlers869312775
pharmgkbrs869312775
gwascentralrs869312775
openSNPrs869312775
23andMers869312775
23andMe allrs869312775
SNP Nexus

SNPshotrs869312775
SNPdbers869312775
MSV3drs869312775
GWAS Ctlgrs869312775
Max Magnitude0
ClinVar
Risk rs869312775(G;G)
Alt rs869312775(G;G)
Reference rs869312775(A;A)
Significance Probable-Pathogenic
Disease Cowden syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000010.10:g.89692860A>G
CLNSRC
CLNACC RCV000210160.1,