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rs786204932

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204932(A;T)
Make rs786204932(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933150
GenePTEN
is asnp
is mentioned by
dbSNPrs786204932
ebirs786204932
HLIrs786204932
Exacrs786204932
Varsomers786204932
Maprs786204932
PheGenIrs786204932
hapmaprs786204932
1000 genomesrs786204932
hgdprs786204932
ensemblrs786204932
gopubmedrs786204932
geneviewrs786204932
scholarrs786204932
googlers786204932
pharmgkbrs786204932
gwascentralrs786204932
openSNPrs786204932
23andMers786204932
23andMe allrs786204932
SNP Nexus

SNPshotrs786204932
SNPdbers786204932
MSV3drs786204932
GWAS Ctlgrs786204932
Max Magnitude0
ClinVar
Risk rs786204932(T;T)
Alt rs786204932(T;T)
Reference rs786204932(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.89692907A>T
CLNSRC
CLNACC RCV000169877.1,