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rs869312779

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312779(-;-)
Make rs869312779(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933183
GenePTEN
is asnp
is mentioned by
dbSNPrs869312779
ebirs869312779
HLIrs869312779
Exacrs869312779
Varsomers869312779
Maprs869312779
PheGenIrs869312779
hapmaprs869312779
1000 genomesrs869312779
hgdprs869312779
ensemblrs869312779
gopubmedrs869312779
geneviewrs869312779
scholarrs869312779
googlers869312779
pharmgkbrs869312779
gwascentralrs869312779
openSNPrs869312779
23andMers869312779
23andMe allrs869312779
SNP Nexus

SNPshotrs869312779
SNPdbers869312779
MSV3drs869312779
GWAS Ctlgrs869312779
Max Magnitude0
ClinVar
Risk rs869312779(;)
Alt rs869312779(;)
Reference rs869312779(C;C)
Significance Pathogenic
Disease Cowden syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000010.10:g.89692940delC
CLNSRC
CLNACC RCV000210072.1,