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rs876661009

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661009(-;-)
Make rs876661009(-;A)
Make rs876661009(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87864516
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs876661009
ebirs876661009
HLIrs876661009
Exacrs876661009
Varsomers876661009
Maprs876661009
PheGenIrs876661009
hapmaprs876661009
1000 genomesrs876661009
hgdprs876661009
ensemblrs876661009
gopubmedrs876661009
geneviewrs876661009
scholarrs876661009
googlers876661009
pharmgkbrs876661009
gwascentralrs876661009
openSNPrs876661009
23andMers876661009
23andMe allrs876661009
SNP Nexus

SNPshotrs876661009
SNPdbers876661009
MSV3drs876661009
GWAS Ctlgrs876661009
Max Magnitude0
ClinVar
Risk rs876661009(A;A)
Alt rs876661009(A;A)
Reference rs876661009(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89624273dupA
CLNSRC
CLNACC RCV000221548.1,