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rs876661177

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661177(G;G)
Make rs876661177(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87931078
GenePTEN
is asnp
is mentioned by
dbSNPrs876661177
ebirs876661177
HLIrs876661177
Exacrs876661177
Varsomers876661177
Maprs876661177
PheGenIrs876661177
hapmaprs876661177
1000 genomesrs876661177
hgdprs876661177
ensemblrs876661177
gopubmedrs876661177
geneviewrs876661177
scholarrs876661177
googlers876661177
pharmgkbrs876661177
gwascentralrs876661177
openSNPrs876661177
23andMers876661177
23andMe allrs876661177
SNP Nexus

SNPshotrs876661177
SNPdbers876661177
MSV3drs876661177
GWAS Ctlgrs876661177
Max Magnitude0
ClinVar
Risk rs876661177(G;G)
Alt rs876661177(G;G)
Reference rs876661177(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89690835T>G
CLNSRC
CLNACC RCV000221920.1,