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rs786204856

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204856(C;T)
Make rs786204856(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933043
GenePTEN
is asnp
is mentioned by
dbSNPrs786204856
ebirs786204856
HLIrs786204856
Exacrs786204856
Varsomers786204856
Maprs786204856
PheGenIrs786204856
hapmaprs786204856
1000 genomesrs786204856
hgdprs786204856
ensemblrs786204856
gopubmedrs786204856
geneviewrs786204856
scholarrs786204856
googlers786204856
pharmgkbrs786204856
gwascentralrs786204856
openSNPrs786204856
23andMers786204856
23andMe allrs786204856
SNP Nexus

SNPshotrs786204856
SNPdbers786204856
MSV3drs786204856
GWAS Ctlgrs786204856
Max Magnitude0
ClinVar
Risk rs786204856(T;T)
Alt rs786204856(T;T)
Reference rs786204856(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692800C>T
CLNSRC
CLNACC RCV000169793.1,