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rs878853012

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853012(G;G)
Make rs878853012(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87952156
GenePTEN
is asnp
is mentioned by
dbSNPrs878853012
ebirs878853012
HLIrs878853012
Exacrs878853012
Varsomers878853012
Maprs878853012
PheGenIrs878853012
hapmaprs878853012
1000 genomesrs878853012
hgdprs878853012
ensemblrs878853012
gopubmedrs878853012
geneviewrs878853012
scholarrs878853012
googlers878853012
pharmgkbrs878853012
gwascentralrs878853012
openSNPrs878853012
23andMers878853012
23andMe allrs878853012
SNP Nexus

SNPshotrs878853012
SNPdbers878853012
MSV3drs878853012
GWAS Ctlgrs878853012
Max Magnitude0
ClinVar
Risk rs878853012(G;G)
Alt rs878853012(G;G)
Reference rs878853012(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89711913T>G
CLNSRC
CLNACC RCV000224211.1,