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rs121909237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121909237(C;G)
Make rs121909237(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87933121
GenePTEN
is asnp
is mentioned by
dbSNPrs121909237
ebirs121909237
HLIrs121909237
Exacrs121909237
Varsomers121909237
Maprs121909237
PheGenIrs121909237
hapmaprs121909237
1000 genomesrs121909237
hgdprs121909237
ensemblrs121909237
gopubmedrs121909237
geneviewrs121909237
scholarrs121909237
googlers121909237
pharmgkbrs121909237
gwascentralrs121909237
openSNPrs121909237
23andMers121909237
23andMe allrs121909237
SNP Nexus

SNPshotrs121909237
SNPdbers121909237
MSV3drs121909237
GWAS Ctlgrs121909237
Max Magnitude0
OMIM601728
Desc
Variant0031
Relatedalso
ClinVar
Risk rs121909237(G;G)
Alt rs121909237(G;G)
Reference rs121909237(C;C)
Significance Pathogenic
Disease Squamous cell carcinoma of the head and neck
Variation info
Gene PTEN
CLNDBN Squamous cell carcinoma of the head and neck
Reversed 0
HGVS NC_000010.10:g.89692878C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008291.4,