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rs876659456

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659456(-;-)
Make rs876659456(-;T)
Make rs876659456(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87952210
GenePTEN
is asnp
is mentioned by
dbSNPrs876659456
ebirs876659456
HLIrs876659456
Exacrs876659456
Varsomers876659456
Maprs876659456
PheGenIrs876659456
hapmaprs876659456
1000 genomesrs876659456
hgdprs876659456
ensemblrs876659456
gopubmedrs876659456
geneviewrs876659456
scholarrs876659456
googlers876659456
pharmgkbrs876659456
gwascentralrs876659456
openSNPrs876659456
23andMers876659456
23andMe allrs876659456
SNP Nexus

SNPshotrs876659456
SNPdbers876659456
MSV3drs876659456
GWAS Ctlgrs876659456
Max Magnitude0
ClinVar
Risk rs876659456(T;T)
Alt rs876659456(T;T)
Reference rs876659456(;)
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.89711967dupT
CLNSRC
CLNACC RCV000214428.1,