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rs786204854

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204854(C;C)
Make rs786204854(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894051
GenePTEN
is asnp
is mentioned by
dbSNPrs786204854
ebirs786204854
HLIrs786204854
Exacrs786204854
Varsomers786204854
Maprs786204854
PheGenIrs786204854
hapmaprs786204854
1000 genomesrs786204854
hgdprs786204854
ensemblrs786204854
gopubmedrs786204854
geneviewrs786204854
scholarrs786204854
googlers786204854
pharmgkbrs786204854
gwascentralrs786204854
openSNPrs786204854
23andMers786204854
23andMe allrs786204854
SNP Nexus

SNPshotrs786204854
SNPdbers786204854
MSV3drs786204854
GWAS Ctlgrs786204854
Max Magnitude0
ClinVar
Risk rs786204854(C;C)
Alt rs786204854(C;C)
Reference rs786204854(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653808G>C
CLNSRC
CLNACC RCV000169789.1,