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rs587776675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776675(G;T)
Make rs587776675(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87863608
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs587776675
ebirs587776675
HLIrs587776675
Exacrs587776675
Varsomers587776675
Maprs587776675
PheGenIrs587776675
hapmaprs587776675
1000 genomesrs587776675
hgdprs587776675
ensemblrs587776675
gopubmedrs587776675
geneviewrs587776675
scholarrs587776675
googlers587776675
pharmgkbrs587776675
gwascentralrs587776675
openSNPrs587776675
23andMers587776675
23andMe allrs587776675
SNP Nexus

SNPshotrs587776675
SNPdbers587776675
MSV3drs587776675
GWAS Ctlgrs587776675
Max Magnitude0
ClinVar
Risk rs587776675(C,T;C,T)
Alt rs587776675(C,T;C,T)
Reference rs587776675(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Cowden syndrome 1
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome Cowden syndrome 1
Reversed 0
HGVS NC_000010.10:g.89623365G>C; NC_000010.10:g.89623365G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000169886.1, RCV000008295.2,