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rs121909235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909235(A;A)
Make rs121909235(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87957919
GenePTEN
is asnp
is mentioned by
dbSNPrs121909235
ebirs121909235
HLIrs121909235
Exacrs121909235
Varsomers121909235
Maprs121909235
PheGenIrs121909235
hapmaprs121909235
1000 genomesrs121909235
hgdprs121909235
ensemblrs121909235
gopubmedrs121909235
geneviewrs121909235
scholarrs121909235
googlers121909235
pharmgkbrs121909235
gwascentralrs121909235
openSNPrs121909235
23andMers121909235
23andMe allrs121909235
SNP Nexus

SNPshotrs121909235
SNPdbers121909235
MSV3drs121909235
GWAS Ctlgrs121909235
Max Magnitude0
OMIM601728
Desc
Variant0029
Relatedalso
ClinVar
Risk rs121909235(A;A)
Alt rs121909235(A;A)
Reference rs121909235(G;G)
Significance Other
Disease Glioma susceptibility 2 Meningioma
Variation info
Gene PTEN
CLNDBN Glioma susceptibility 2 Meningioma
Reversed 0
HGVS NC_000010.10:g.89717676G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008288.2, RCV000008289.2,