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rs786204884

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204884(-;-)
Make rs786204884(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960984
GenePTEN
is asnp
is mentioned by
dbSNPrs786204884
ebirs786204884
HLIrs786204884
Exacrs786204884
Varsomers786204884
Maprs786204884
PheGenIrs786204884
hapmaprs786204884
1000 genomesrs786204884
hgdprs786204884
ensemblrs786204884
gopubmedrs786204884
geneviewrs786204884
scholarrs786204884
googlers786204884
pharmgkbrs786204884
gwascentralrs786204884
openSNPrs786204884
23andMers786204884
23andMe allrs786204884
SNP Nexus

SNPshotrs786204884
SNPdbers786204884
MSV3drs786204884
GWAS Ctlgrs786204884
Max Magnitude0
ClinVar
Risk rs786204884(;)
Alt rs786204884(;)
Reference rs786204884(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720741delC
CLNSRC
CLNACC RCV000169825.1,