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rs876661010

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661010(A;C)
Make rs876661010(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87864545
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs876661010
ebirs876661010
HLIrs876661010
Exacrs876661010
Varsomers876661010
Maprs876661010
PheGenIrs876661010
hapmaprs876661010
1000 genomesrs876661010
hgdprs876661010
ensemblrs876661010
gopubmedrs876661010
geneviewrs876661010
scholarrs876661010
googlers876661010
pharmgkbrs876661010
gwascentralrs876661010
openSNPrs876661010
23andMers876661010
23andMe allrs876661010
SNP Nexus

SNPshotrs876661010
SNPdbers876661010
MSV3drs876661010
GWAS Ctlgrs876661010
Max Magnitude0
ClinVar
Risk rs876661010(C;C)
Alt rs876661010(C;C)
Reference rs876661010(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89624302A>C
CLNSRC
CLNACC RCV000217854.1,