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rs876661058

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661058(A;A)
Make rs876661058(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87961037
GenePTEN
is asnp
is mentioned by
dbSNPrs876661058
ebirs876661058
HLIrs876661058
Exacrs876661058
Varsomers876661058
Maprs876661058
PheGenIrs876661058
hapmaprs876661058
1000 genomesrs876661058
hgdprs876661058
ensemblrs876661058
gopubmedrs876661058
geneviewrs876661058
scholarrs876661058
googlers876661058
pharmgkbrs876661058
gwascentralrs876661058
openSNPrs876661058
23andMers876661058
23andMe allrs876661058
SNP Nexus

SNPshotrs876661058
SNPdbers876661058
MSV3drs876661058
GWAS Ctlgrs876661058
Max Magnitude0
ClinVar
Risk rs876661058(A;A)
Alt rs876661058(A;A)
Reference rs876661058(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89720794T>A
CLNSRC
CLNACC RCV000222109.1,