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rs121909223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909223(C;C)
Make rs121909223(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87933129
GenePTEN
is asnp
is mentioned by
dbSNPrs121909223
ebirs121909223
HLIrs121909223
Exacrs121909223
Varsomers121909223
Maprs121909223
PheGenIrs121909223
hapmaprs121909223
1000 genomesrs121909223
hgdprs121909223
ensemblrs121909223
gopubmedrs121909223
geneviewrs121909223
scholarrs121909223
googlers121909223
pharmgkbrs121909223
gwascentralrs121909223
openSNPrs121909223
23andMers121909223
23andMe allrs121909223
SNP Nexus

SNPshotrs121909223
SNPdbers121909223
MSV3drs121909223
GWAS Ctlgrs121909223
Max Magnitude0
OMIM601728
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909223(C,G;C,G)
Alt rs121909223(C,G;C,G)
Reference rs121909223(T;T)
Significance Pathogenic
Disease Cowden syndrome 1 Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692886T>C; NC_000010.10:g.89692886T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008261.2, RCV000165307.1,