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rs786204905

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204905(-;-)
Make rs786204905(-;A)
Make rs786204905(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960967
GenePTEN
is asnp
is mentioned by
dbSNPrs786204905
ebirs786204905
HLIrs786204905
Exacrs786204905
Varsomers786204905
Maprs786204905
PheGenIrs786204905
hapmaprs786204905
1000 genomesrs786204905
hgdprs786204905
ensemblrs786204905
gopubmedrs786204905
geneviewrs786204905
scholarrs786204905
googlers786204905
pharmgkbrs786204905
gwascentralrs786204905
openSNPrs786204905
23andMers786204905
23andMe allrs786204905
SNP Nexus

SNPshotrs786204905
SNPdbers786204905
MSV3drs786204905
GWAS Ctlgrs786204905
Max Magnitude0
ClinVar
Risk rs786204905(A;A)
Alt rs786204905(A;A)
Reference rs786204905(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720724dupA
CLNSRC
CLNACC RCV000169846.1,