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rs121909234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909234(A;A)
Make rs121909234(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87957867
GenePTEN
is asnp
is mentioned by
dbSNPrs121909234
ebirs121909234
HLIrs121909234
Exacrs121909234
Varsomers121909234
Maprs121909234
PheGenIrs121909234
hapmaprs121909234
1000 genomesrs121909234
hgdprs121909234
ensemblrs121909234
gopubmedrs121909234
geneviewrs121909234
scholarrs121909234
googlers121909234
pharmgkbrs121909234
gwascentralrs121909234
openSNPrs121909234
23andMers121909234
23andMe allrs121909234
SNP Nexus

SNPshotrs121909234
SNPdbers121909234
MSV3drs121909234
GWAS Ctlgrs121909234
Max Magnitude0
OMIM601728
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121909234(A;A)
Alt rs121909234(A;A)
Reference rs121909234(G;G)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene PTEN
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000010.10:g.89717624G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008286.4,