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rs786204892

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204892(-;-)
Make rs786204892(-;A)
Make rs786204892(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87961047
GenePTEN
is asnp
is mentioned by
dbSNPrs786204892
ebirs786204892
HLIrs786204892
Exacrs786204892
Varsomers786204892
Maprs786204892
PheGenIrs786204892
hapmaprs786204892
1000 genomesrs786204892
hgdprs786204892
ensemblrs786204892
gopubmedrs786204892
geneviewrs786204892
scholarrs786204892
googlers786204892
pharmgkbrs786204892
gwascentralrs786204892
openSNPrs786204892
23andMers786204892
23andMe allrs786204892
SNP Nexus

SNPshotrs786204892
SNPdbers786204892
MSV3drs786204892
GWAS Ctlgrs786204892
Max Magnitude0
ClinVar
Risk rs786204892(A;A)
Alt rs786204892(A;A)
Reference rs786204892(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720804dupA
CLNSRC
CLNACC RCV000169833.1,