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rs876658153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6.3 Hereditary cancer predisposing syndrome
(G;G) 0 common in clinvar
Make rs876658153(G;T)
Make rs876658153(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925558
GenePTEN
is asnp
is mentioned by
dbSNPrs876658153
dbSNP (classic)rs876658153
ClinGenrs876658153
ebirs876658153
HLIrs876658153
Exacrs876658153
Gnomadrs876658153
Varsomers876658153
LitVarrs876658153
Maprs876658153
PheGenIrs876658153
Biobankrs876658153
1000 genomesrs876658153
hgdprs876658153
ensemblrs876658153
geneviewrs876658153
scholarrs876658153
googlers876658153
pharmgkbrs876658153
gwascentralrs876658153
openSNPrs876658153
23andMers876658153
SNPshotrs876658153
SNPdbers876658153
MSV3drs876658153
GWAS Ctlgrs876658153
Max Magnitude6.3
ClinVar
Risk rs876658153(A;A) rs876658153(T;T)
Alt rs876658153(A;A) rs876658153(T;T)
Reference Rs876658153(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89685315G>A; NC_000010.10:g.89685315G>T
CLNSRC
CLNACC RCV000482154.1, RCV000491897.1, RCV000213295.1,