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rs786202517

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs786202517(AC;AC)
Make rs786202517(AC;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894050
GenePTEN
is asnp
is mentioned by
dbSNPrs786202517
ebirs786202517
HLIrs786202517
Exacrs786202517
Varsomers786202517
Maprs786202517
PheGenIrs786202517
hapmaprs786202517
1000 genomesrs786202517
hgdprs786202517
ensemblrs786202517
gopubmedrs786202517
geneviewrs786202517
scholarrs786202517
googlers786202517
pharmgkbrs786202517
gwascentralrs786202517
openSNPrs786202517
23andMers786202517
23andMe allrs786202517
SNP Nexus

SNPshotrs786202517
SNPdbers786202517
MSV3drs786202517
GWAS Ctlgrs786202517
Max Magnitude0
ClinVar
Risk rs786202517(AC;AC)
Alt rs786202517(AC;AC)
Reference rs786202517(GG;GG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653807_89653808delGGinsAC
CLNSRC
CLNACC RCV000165361.1,