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

rs786204894

From SNPedia

Orientationplus
Geno Mag Summary
(TATC;TATC) 0 common in clinvar
Make rs786204894(-;-)
Make rs786204894(-;TATC)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894030
GenePTEN
is asnp
is mentioned by
dbSNPrs786204894
ebirs786204894
HLIrs786204894
Exacrs786204894
Varsomers786204894
Maprs786204894
PheGenIrs786204894
hapmaprs786204894
1000 genomesrs786204894
hgdprs786204894
ensemblrs786204894
gopubmedrs786204894
geneviewrs786204894
scholarrs786204894
googlers786204894
pharmgkbrs786204894
gwascentralrs786204894
openSNPrs786204894
23andMers786204894
23andMe allrs786204894
SNP Nexus

SNPshotrs786204894
SNPdbers786204894
MSV3drs786204894
GWAS Ctlgrs786204894
Max Magnitude0
ClinVar
Risk rs786204894(;)
Alt rs786204894(;)
Reference rs786204894(TATC;TATC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653787_89653790delTATC
CLNSRC
CLNACC RCV000169835.1,