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rs121913290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AA) 6.3 Hereditary cancer predisposing syndrome
(AA;AA) 0 common in clinvar


Make rs121913290(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87864486
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs121913290
dbSNP (old)rs121913290
ClinGenrs121913290
ebirs121913290
HLIrs121913290
Exacrs121913290
Gnomadrs121913290
Varsomers121913290
Maprs121913290
PheGenIrs121913290
Biobankrs121913290
1000 genomesrs121913290
hgdprs121913290
ensemblrs121913290
gopubmedrs121913290
geneviewrs121913290
scholarrs121913290
googlers121913290
pharmgkbrs121913290
gwascentralrs121913290
openSNPrs121913290
23andMers121913290
23andMe allrs121913290
SNP Nexus

SNPshotrs121913290
SNPdbers121913290
MSV3drs121913290
GWAS Ctlgrs121913290
Max Magnitude6.3
ClinVar
Risk rs121913290(-;-)
Alt rs121913290(-;-)
Reference Rs121913290(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89624243_89624244delAA
CLNSRC
CLNACC RCV000215567.1, RCV000222693.1,