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rs869312778

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312778(G;T)
Make rs869312778(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894063
GenePTEN
is asnp
is mentioned by
dbSNPrs869312778
ebirs869312778
HLIrs869312778
Exacrs869312778
Varsomers869312778
Maprs869312778
PheGenIrs869312778
hapmaprs869312778
1000 genomesrs869312778
hgdprs869312778
ensemblrs869312778
gopubmedrs869312778
geneviewrs869312778
scholarrs869312778
googlers869312778
pharmgkbrs869312778
gwascentralrs869312778
openSNPrs869312778
23andMers869312778
23andMe allrs869312778
SNP Nexus

SNPshotrs869312778
SNPdbers869312778
MSV3drs869312778
GWAS Ctlgrs869312778
Max Magnitude0
ClinVar
Risk rs869312778(T;T)
Alt rs869312778(T;T)
Reference rs869312778(G;G)
Significance Pathogenic
Disease Cowden syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000010.10:g.89653820G>T
CLNSRC
CLNACC RCV000210162.1,