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rs786202894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;GCGT) 6.3 Hereditary cancer predisposing syndrome
Make rs786202894(GCGT;GCGT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894079
GenePTEN
is asnp
is mentioned by
dbSNPrs786202894
dbSNP (old)rs786202894
ClinGenrs786202894
ebirs786202894
HLIrs786202894
Exacrs786202894
Gnomadrs786202894
Varsomers786202894
Maprs786202894
PheGenIrs786202894
Biobankrs786202894
1000 genomesrs786202894
hgdprs786202894
ensemblrs786202894
gopubmedrs786202894
geneviewrs786202894
scholarrs786202894
googlers786202894
pharmgkbrs786202894
gwascentralrs786202894
openSNPrs786202894
23andMers786202894
23andMe allrs786202894
SNP Nexus

SNPshotrs786202894
SNPdbers786202894
MSV3drs786202894
GWAS Ctlgrs786202894
Max Magnitude6.3
ClinVar
Risk rs786202894(GCGT;GCGT)
Alt rs786202894(GCGT;GCGT)
Reference Rs786202894(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653833_89653836dupGCGT
CLNSRC
CLNACC RCV000165953.1,