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rs121913294

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913294(A;A)
Make rs121913294(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952143
GenePTEN
is asnp
is mentioned by
dbSNPrs121913294
ebirs121913294
HLIrs121913294
Exacrs121913294
Varsomers121913294
Maprs121913294
PheGenIrs121913294
hapmaprs121913294
1000 genomesrs121913294
hgdprs121913294
ensemblrs121913294
gopubmedrs121913294
geneviewrs121913294
scholarrs121913294
googlers121913294
pharmgkbrs121913294
gwascentralrs121913294
openSNPrs121913294
23andMers121913294
23andMe allrs121913294
SNP Nexus

SNPshotrs121913294
SNPdbers121913294
MSV3drs121913294
GWAS Ctlgrs121913294
Max Magnitude0
ClinVar
Risk rs121913294(A,C;A,C)
Alt rs121913294(A,C;A,C)
Reference rs121913294(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711900G>C
CLNSRC
CLNACC RCV000164565.1,