Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853940

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853940(-;-)
Make rs878853940(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87864522
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs878853940
ebirs878853940
HLIrs878853940
Exacrs878853940
Varsomers878853940
Maprs878853940
PheGenIrs878853940
hapmaprs878853940
1000 genomesrs878853940
hgdprs878853940
ensemblrs878853940
gopubmedrs878853940
geneviewrs878853940
scholarrs878853940
googlers878853940
pharmgkbrs878853940
gwascentralrs878853940
openSNPrs878853940
23andMers878853940
23andMe allrs878853940
SNP Nexus

SNPshotrs878853940
SNPdbers878853940
MSV3drs878853940
GWAS Ctlgrs878853940
Max Magnitude0
ClinVar
Risk rs878853940(;)
Alt rs878853940(;)
Reference rs878853940(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89624279delA
CLNSRC
CLNACC RCV000227851.1,