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rs121909233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909233(A;A)
Make rs121909233(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87864524
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs121909233
ebirs121909233
HLIrs121909233
Exacrs121909233
Varsomers121909233
Maprs121909233
PheGenIrs121909233
hapmaprs121909233
1000 genomesrs121909233
hgdprs121909233
ensemblrs121909233
gopubmedrs121909233
geneviewrs121909233
scholarrs121909233
googlers121909233
pharmgkbrs121909233
gwascentralrs121909233
openSNPrs121909233
23andMers121909233
23andMe allrs121909233
SNP Nexus

SNPshotrs121909233
SNPdbers121909233
MSV3drs121909233
GWAS Ctlgrs121909233
Max Magnitude0
OMIM601728
Desc
Variant0025
Relatedalso
ClinVar
Risk rs121909233(A;A)
Alt rs121909233(A;A)
Reference rs121909233(G;G)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000010.10:g.89624281G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008285.4,