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rs876658171

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs876658171(-;-)
Make rs876658171(-;AT)
Make rs876658171(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894042
GenePTEN
is asnp
is mentioned by
dbSNPrs876658171
ebirs876658171
HLIrs876658171
Exacrs876658171
Varsomers876658171
Maprs876658171
PheGenIrs876658171
hapmaprs876658171
1000 genomesrs876658171
hgdprs876658171
ensemblrs876658171
gopubmedrs876658171
geneviewrs876658171
scholarrs876658171
googlers876658171
pharmgkbrs876658171
gwascentralrs876658171
openSNPrs876658171
23andMers876658171
23andMe allrs876658171
SNP Nexus

SNPshotrs876658171
SNPdbers876658171
MSV3drs876658171
GWAS Ctlgrs876658171
Max Magnitude0
ClinVar
Risk rs876658171(;)
Alt rs876658171(;)
Reference rs876658171(TA;TA)
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.89653799_89653800delAT
CLNSRC
CLNACC RCV000213398.1,