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rs587776674

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776674(A;A)
Make rs587776674(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position87863705
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs587776674
ebirs587776674
HLIrs587776674
Exacrs587776674
Varsomers587776674
Maprs587776674
PheGenIrs587776674
hapmaprs587776674
1000 genomesrs587776674
hgdprs587776674
ensemblrs587776674
gopubmedrs587776674
geneviewrs587776674
scholarrs587776674
googlers587776674
pharmgkbrs587776674
gwascentralrs587776674
openSNPrs587776674
23andMers587776674
23andMe allrs587776674
SNP Nexus

SNPshotrs587776674
SNPdbers587776674
MSV3drs587776674
GWAS Ctlgrs587776674
Max Magnitude0
ClinVar
Risk rs587776674(A;A)
Alt rs587776674(A;A)
Reference rs587776674(G;G)
Significance Pathogenic
Disease Cowden syndrome 1 not specified PTEN hamartoma tumor syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Cowden syndrome 1 not specified PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89623462G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008294.2, RCV000169801.1, RCV000230941.1,