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rs786204902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;AT) 6.3 Hereditary cancer predisposing syndrome
Make rs786204902(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957957
GenePTEN
is asnp
is mentioned by
dbSNPrs786204902
dbSNP (old)rs786204902
ClinGenrs786204902
ebirs786204902
HLIrs786204902
Exacrs786204902
Gnomadrs786204902
Varsomers786204902
Maprs786204902
PheGenIrs786204902
Biobankrs786204902
1000 genomesrs786204902
hgdprs786204902
ensemblrs786204902
gopubmedrs786204902
geneviewrs786204902
scholarrs786204902
googlers786204902
pharmgkbrs786204902
gwascentralrs786204902
openSNPrs786204902
23andMers786204902
23andMe allrs786204902
SNP Nexus

SNPshotrs786204902
SNPdbers786204902
MSV3drs786204902
GWAS Ctlgrs786204902
Max Magnitude6.3
ClinVar
Risk rs786204902(TA;TA)
Alt rs786204902(TA;TA)
Reference Rs786204902(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717714_89717715insAT
CLNSRC
CLNACC RCV000169843.1,