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rs786204859

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204859(A;A)
Make rs786204859(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933166
GenePTEN
is asnp
is mentioned by
dbSNPrs786204859
ebirs786204859
HLIrs786204859
Exacrs786204859
Varsomers786204859
Maprs786204859
PheGenIrs786204859
hapmaprs786204859
1000 genomesrs786204859
hgdprs786204859
ensemblrs786204859
gopubmedrs786204859
geneviewrs786204859
scholarrs786204859
googlers786204859
pharmgkbrs786204859
gwascentralrs786204859
openSNPrs786204859
23andMers786204859
23andMe allrs786204859
SNP Nexus

SNPshotrs786204859
SNPdbers786204859
MSV3drs786204859
GWAS Ctlgrs786204859
Max Magnitude0
ClinVar
Risk rs786204859(A;A)
Alt rs786204859(A;A)
Reference rs786204859(G;G)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89692923G>A
CLNSRC
CLNACC RCV000169797.2, RCV000217011.1,