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rs876658304

From SNPedia

Orientationplus
Geno Mag Summary
(ATTT;ATTT) 0 common in clinvar
Make rs876658304(-;-)
Make rs876658304(-;ATTT)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87933217
GenePTEN
is asnp
is mentioned by
dbSNPrs876658304
ebirs876658304
HLIrs876658304
Exacrs876658304
Varsomers876658304
Maprs876658304
PheGenIrs876658304
hapmaprs876658304
1000 genomesrs876658304
hgdprs876658304
ensemblrs876658304
gopubmedrs876658304
geneviewrs876658304
scholarrs876658304
googlers876658304
pharmgkbrs876658304
gwascentralrs876658304
openSNPrs876658304
23andMers876658304
23andMe allrs876658304
SNP Nexus

SNPshotrs876658304
SNPdbers876658304
MSV3drs876658304
GWAS Ctlgrs876658304
Max Magnitude0
ClinVar
Risk rs876658304(;)
Alt rs876658304(;)
Reference rs876658304(ATTT;ATTT)
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.89692974_89692977delATTT
CLNSRC
CLNACC RCV000219850.1,