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rs587776668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776668(G;G)
Make rs587776668(G;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87933253
GenePTEN
is asnp
is mentioned by
dbSNPrs587776668
ebirs587776668
HLIrs587776668
Exacrs587776668
Varsomers587776668
Maprs587776668
PheGenIrs587776668
hapmaprs587776668
1000 genomesrs587776668
hgdprs587776668
ensemblrs587776668
gopubmedrs587776668
geneviewrs587776668
scholarrs587776668
googlers587776668
pharmgkbrs587776668
gwascentralrs587776668
openSNPrs587776668
23andMers587776668
23andMe allrs587776668
SNP Nexus

SNPshotrs587776668
SNPdbers587776668
MSV3drs587776668
GWAS Ctlgrs587776668
Max Magnitude0
ClinVar
Risk rs587776668(G;G)
Alt rs587776668(G;G)
Reference rs587776668(T;T)
Significance Pathogenic
Disease not provided Cowden syndrome 1
Variation info
Gene PTEN
CLNDBN not provided Cowden syndrome 1
Reversed 0
HGVS NC_000010.10:g.89693010T>C; NC_000010.10:g.89693010T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000213348.1, RCV000008267.3,