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rs876660634

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660634(A;G)
Make rs876660634(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87925551
GenePTEN
is asnp
is mentioned by
dbSNPrs876660634
ebirs876660634
HLIrs876660634
Exacrs876660634
Varsomers876660634
Maprs876660634
PheGenIrs876660634
hapmaprs876660634
1000 genomesrs876660634
hgdprs876660634
ensemblrs876660634
gopubmedrs876660634
geneviewrs876660634
scholarrs876660634
googlers876660634
pharmgkbrs876660634
gwascentralrs876660634
openSNPrs876660634
23andMers876660634
23andMe allrs876660634
SNP Nexus

SNPshotrs876660634
SNPdbers876660634
MSV3drs876660634
GWAS Ctlgrs876660634
Max Magnitude0
ClinVar
Risk rs876660634(G;G)
Alt rs876660634(G;G)
Reference rs876660634(A;A)
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.89685308A>G
CLNSRC
CLNACC RCV000215167.1,