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rs121909220

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909220(G;T)
Make rs121909220(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87933228
GenePTEN
is asnp
is mentioned by
dbSNPrs121909220
ebirs121909220
HLIrs121909220
Exacrs121909220
Varsomers121909220
Maprs121909220
PheGenIrs121909220
hapmaprs121909220
1000 genomesrs121909220
hgdprs121909220
ensemblrs121909220
gopubmedrs121909220
geneviewrs121909220
scholarrs121909220
googlers121909220
pharmgkbrs121909220
gwascentralrs121909220
openSNPrs121909220
23andMers121909220
23andMe allrs121909220
SNP Nexus

SNPshotrs121909220
SNPdbers121909220
MSV3drs121909220
GWAS Ctlgrs121909220
Max Magnitude0
OMIM601728
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909220(T;T)
Alt rs121909220(T;T)
Reference rs121909220(G;G)
Significance Pathogenic
Disease Lhermitte-Duclos disease
Variation info
Gene PTEN
CLNDBN Lhermitte-Duclos disease
Reversed 0
HGVS NC_000010.10:g.89692985G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008258.2,