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rs786204867

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204867(C;C)
Make rs786204867(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952224
GenePTEN
is asnp
is mentioned by
dbSNPrs786204867
ebirs786204867
HLIrs786204867
Exacrs786204867
Varsomers786204867
Maprs786204867
PheGenIrs786204867
hapmaprs786204867
1000 genomesrs786204867
hgdprs786204867
ensemblrs786204867
gopubmedrs786204867
geneviewrs786204867
scholarrs786204867
googlers786204867
pharmgkbrs786204867
gwascentralrs786204867
openSNPrs786204867
23andMers786204867
23andMe allrs786204867
SNP Nexus

SNPshotrs786204867
SNPdbers786204867
MSV3drs786204867
GWAS Ctlgrs786204867
Max Magnitude0
ClinVar
Risk rs786204867(C;C)
Alt rs786204867(C;C)
Reference rs786204867(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89711981T>C
CLNSRC
CLNACC RCV000169807.2,