Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204899

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204899(-;-)
Make rs786204899(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933080
GenePTEN
is asnp
is mentioned by
dbSNPrs786204899
ebirs786204899
HLIrs786204899
Exacrs786204899
Varsomers786204899
Maprs786204899
PheGenIrs786204899
hapmaprs786204899
1000 genomesrs786204899
hgdprs786204899
ensemblrs786204899
gopubmedrs786204899
geneviewrs786204899
scholarrs786204899
googlers786204899
pharmgkbrs786204899
gwascentralrs786204899
openSNPrs786204899
23andMers786204899
23andMe allrs786204899
SNP Nexus

SNPshotrs786204899
SNPdbers786204899
MSV3drs786204899
GWAS Ctlgrs786204899
Max Magnitude0
ClinVar
Risk rs786204899(;)
Alt rs786204899(;)
Reference rs786204899(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692837delT
CLNSRC
CLNACC RCV000169840.1,