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rs762518389

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762518389(C;T)
Make rs762518389(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894089
GenePTEN
is asnp
is mentioned by
dbSNPrs762518389
ebirs762518389
HLIrs762518389
Exacrs762518389
Varsomers762518389
Maprs762518389
PheGenIrs762518389
hapmaprs762518389
1000 genomesrs762518389
hgdprs762518389
ensemblrs762518389
gopubmedrs762518389
geneviewrs762518389
scholarrs762518389
googlers762518389
pharmgkbrs762518389
gwascentralrs762518389
openSNPrs762518389
23andMers762518389
23andMe allrs762518389
SNP Nexus

SNPshotrs762518389
SNPdbers762518389
MSV3drs762518389
GWAS Ctlgrs762518389
Max Magnitude0
ClinVar
Risk rs762518389(T;T)
Alt rs762518389(T;T)
Reference rs762518389(C;C)
Significance Probable-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.89653846C>G
CLNSRC
CLNACC RCV000213950.1,