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rs876660082

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660082(-;-)
Make rs876660082(-;G)
Make rs876660082(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87931090
GenePTEN
is asnp
is mentioned by
dbSNPrs876660082
ebirs876660082
HLIrs876660082
Exacrs876660082
Varsomers876660082
Maprs876660082
PheGenIrs876660082
hapmaprs876660082
1000 genomesrs876660082
hgdprs876660082
ensemblrs876660082
gopubmedrs876660082
geneviewrs876660082
scholarrs876660082
googlers876660082
pharmgkbrs876660082
gwascentralrs876660082
openSNPrs876660082
23andMers876660082
23andMe allrs876660082
SNP Nexus

SNPshotrs876660082
SNPdbers876660082
MSV3drs876660082
GWAS Ctlgrs876660082
Max Magnitude0
ClinVar
Risk rs876660082(G;G)
Alt rs876660082(G;G)
Reference rs876660082(;)
Significance 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.89690847dupG
CLNSRC
CLNACC RCV000214537.1,