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rs587783058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6.3 Cowden syndrome
Make rs587783058(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87961060
GenePTEN
is asnp
is mentioned by
dbSNPrs587783058
dbSNP (old)rs587783058
ClinGenrs587783058
ebirs587783058
HLIrs587783058
Exacrs587783058
Varsomers587783058
Maprs587783058
PheGenIrs587783058
Biobankrs587783058
1000 genomesrs587783058
hgdprs587783058
ensemblrs587783058
gopubmedrs587783058
geneviewrs587783058
scholarrs587783058
googlers587783058
pharmgkbrs587783058
gwascentralrs587783058
openSNPrs587783058
23andMers587783058
23andMe allrs587783058
SNP Nexus

SNPshotrs587783058
SNPdbers587783058
MSV3drs587783058
GWAS Ctlgrs587783058
Max Magnitude6.3
ClinVar
Risk rs587783058(A;A)
Alt rs587783058(A;A)
Reference Rs587783058(-;-)
Significance Pathogenic
Disease Cowden syndrome 1 not provided
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1 not provided
Reversed 0
HGVS NC_000010.10:g.89720817dupA
CLNSRC
CLNACC RCV000144658.1, RCV000479366.1,