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rs786204857

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204857(A;T)
Make rs786204857(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933060
GenePTEN
is asnp
is mentioned by
dbSNPrs786204857
ebirs786204857
HLIrs786204857
Exacrs786204857
Varsomers786204857
Maprs786204857
PheGenIrs786204857
hapmaprs786204857
1000 genomesrs786204857
hgdprs786204857
ensemblrs786204857
gopubmedrs786204857
geneviewrs786204857
scholarrs786204857
googlers786204857
pharmgkbrs786204857
gwascentralrs786204857
openSNPrs786204857
23andMers786204857
23andMe allrs786204857
SNP Nexus

SNPshotrs786204857
SNPdbers786204857
MSV3drs786204857
GWAS Ctlgrs786204857
Max Magnitude0
ClinVar
Risk rs786204857(T;T)
Alt rs786204857(T;T)
Reference rs786204857(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692817A>T
CLNSRC
CLNACC RCV000169795.1,