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rs876660535

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660535(A;A)
Make rs876660535(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933130
GenePTEN
is asnp
is mentioned by
dbSNPrs876660535
ebirs876660535
HLIrs876660535
Exacrs876660535
Varsomers876660535
Maprs876660535
PheGenIrs876660535
hapmaprs876660535
1000 genomesrs876660535
hgdprs876660535
ensemblrs876660535
gopubmedrs876660535
geneviewrs876660535
scholarrs876660535
googlers876660535
pharmgkbrs876660535
gwascentralrs876660535
openSNPrs876660535
23andMers876660535
23andMe allrs876660535
SNP Nexus

SNPshotrs876660535
SNPdbers876660535
MSV3drs876660535
GWAS Ctlgrs876660535
Max Magnitude0
ClinVar
Risk rs876660535(A;A)
Alt rs876660535(A;A)
Reference rs876660535(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89692887G>A
CLNSRC
CLNACC RCV000220547.1,