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rs786204890

From SNPedia

Orientationplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs786204890(AAG;T)
Make rs786204890(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952172
GenePTEN
is asnp
is mentioned by
dbSNPrs786204890
ebirs786204890
HLIrs786204890
Exacrs786204890
Varsomers786204890
Maprs786204890
PheGenIrs786204890
hapmaprs786204890
1000 genomesrs786204890
hgdprs786204890
ensemblrs786204890
gopubmedrs786204890
geneviewrs786204890
scholarrs786204890
googlers786204890
pharmgkbrs786204890
gwascentralrs786204890
openSNPrs786204890
23andMers786204890
23andMe allrs786204890
SNP Nexus

SNPshotrs786204890
SNPdbers786204890
MSV3drs786204890
GWAS Ctlgrs786204890
Max Magnitude0
ClinVar
Risk rs786204890(T;T)
Alt rs786204890(T;T)
Reference rs786204890(AAG;AAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711929_89711931delAAGinsT
CLNSRC
CLNACC RCV000169831.1,