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rs121909219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909219(C;T)
Make rs121909219(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87957915
GenePTEN
is asnp
is mentioned by
dbSNPrs121909219
ebirs121909219
HLIrs121909219
Exacrs121909219
Varsomers121909219
Maprs121909219
PheGenIrs121909219
hapmaprs121909219
1000 genomesrs121909219
hgdprs121909219
ensemblrs121909219
gopubmedrs121909219
geneviewrs121909219
scholarrs121909219
googlers121909219
pharmgkbrs121909219
gwascentralrs121909219
openSNPrs121909219
23andMers121909219
23andMe allrs121909219
SNP Nexus

SNPshotrs121909219
SNPdbers121909219
MSV3drs121909219
GWAS Ctlgrs121909219
Max Magnitude0
OMIM601728
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909219(T;T)
Alt rs121909219(T;T)
Reference rs121909219(C;C)
Significance Pathogenic
Disease Cowden syndrome 1 Bannayan-Riley-Ruvalcaba syndrome PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Cowden syndrome 1 Bannayan-Riley-Ruvalcaba syndrome PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89717672C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008256.2, RCV000008257.2, RCV000128455.2, RCV000162649.3, RCV000212882.1,