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rs876661024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;G) 6.3 Hereditary cancer predisposing syndrome
(G;G) 0 common in clinvar


Make rs876661024(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87957852
GenePTEN
is asnp
is mentioned by
dbSNPrs876661024
dbSNP (old)rs876661024
ClinGenrs876661024
ebirs876661024
HLIrs876661024
Exacrs876661024
Gnomadrs876661024
Varsomers876661024
Maprs876661024
PheGenIrs876661024
Biobankrs876661024
1000 genomesrs876661024
hgdprs876661024
ensemblrs876661024
gopubmedrs876661024
geneviewrs876661024
scholarrs876661024
googlers876661024
pharmgkbrs876661024
gwascentralrs876661024
openSNPrs876661024
23andMers876661024
23andMe allrs876661024
SNP Nexus

SNPshotrs876661024
SNPdbers876661024
MSV3drs876661024
GWAS Ctlgrs876661024
Max Magnitude6.3
ClinVar
Risk rs876661024(A;A) rs876661024(C;C)
Alt rs876661024(A;A) rs876661024(C;C)
Reference Rs876661024(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome not provided
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89717609G>A; NC_000010.10:g.89717609G>C
CLNSRC
CLNACC RCV000490578.1, RCV000221132.1,