Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776672(-;-)
Make rs587776672(-;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position87960894
GenePTEN
is asnp
is mentioned by
dbSNPrs587776672
ebirs587776672
HLIrs587776672
Exacrs587776672
Varsomers587776672
Maprs587776672
PheGenIrs587776672
hapmaprs587776672
1000 genomesrs587776672
hgdprs587776672
ensemblrs587776672
gopubmedrs587776672
geneviewrs587776672
scholarrs587776672
googlers587776672
pharmgkbrs587776672
gwascentralrs587776672
openSNPrs587776672
23andMers587776672
23andMe allrs587776672
SNP Nexus

SNPshotrs587776672
SNPdbers587776672
MSV3drs587776672
GWAS Ctlgrs587776672
Max Magnitude0
ClinVar
Risk rs587776672(;)
Alt rs587776672(;)
Reference rs587776672(G;G)
Significance Pathogenic
Disease Cowden syndrome 1
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1
Reversed 0
HGVS NC_000010.10:g.89720651delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000008287.3,