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rs786204927

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204927(C;G)
Make rs786204927(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933036
GenePTEN
is asnp
is mentioned by
dbSNPrs786204927
ebirs786204927
HLIrs786204927
Exacrs786204927
Varsomers786204927
Maprs786204927
PheGenIrs786204927
hapmaprs786204927
1000 genomesrs786204927
hgdprs786204927
ensemblrs786204927
gopubmedrs786204927
geneviewrs786204927
scholarrs786204927
googlers786204927
pharmgkbrs786204927
gwascentralrs786204927
openSNPrs786204927
23andMers786204927
23andMe allrs786204927
SNP Nexus

SNPshotrs786204927
SNPdbers786204927
MSV3drs786204927
GWAS Ctlgrs786204927
Max Magnitude0
ClinVar
Risk rs786204927(G;G)
Alt rs786204927(G;G)
Reference rs786204927(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.89692793C>G
CLNSRC
CLNACC RCV000169872.1,