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rs786204922

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204922(A;G)
Make rs786204922(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87925554
GenePTEN
is asnp
is mentioned by
dbSNPrs786204922
ebirs786204922
HLIrs786204922
Exacrs786204922
Varsomers786204922
Maprs786204922
PheGenIrs786204922
hapmaprs786204922
1000 genomesrs786204922
hgdprs786204922
ensemblrs786204922
gopubmedrs786204922
geneviewrs786204922
scholarrs786204922
googlers786204922
pharmgkbrs786204922
gwascentralrs786204922
openSNPrs786204922
23andMers786204922
23andMe allrs786204922
SNP Nexus

SNPshotrs786204922
SNPdbers786204922
MSV3drs786204922
GWAS Ctlgrs786204922
Max Magnitude0
ClinVar
Risk rs786204922(G;G)
Alt rs786204922(G;G)
Reference rs786204922(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene PTEN
CLNDBN not specified
Reversed 0
HGVS NC_000010.10:g.89685311A>G
CLNSRC
CLNACC RCV000169866.1,