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rs786204915

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204915(A;G)
Make rs786204915(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894082
GenePTEN
is asnp
is mentioned by
dbSNPrs786204915
ebirs786204915
HLIrs786204915
Exacrs786204915
Varsomers786204915
Maprs786204915
PheGenIrs786204915
hapmaprs786204915
1000 genomesrs786204915
hgdprs786204915
ensemblrs786204915
gopubmedrs786204915
geneviewrs786204915
scholarrs786204915
googlers786204915
pharmgkbrs786204915
gwascentralrs786204915
openSNPrs786204915
23andMers786204915
23andMe allrs786204915
SNP Nexus

SNPshotrs786204915
SNPdbers786204915
MSV3drs786204915
GWAS Ctlgrs786204915
Max Magnitude0
ClinVar
Risk rs786204915(G;G)
Alt rs786204915(G;G)
Reference rs786204915(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653839A>G
CLNSRC
CLNACC RCV000169856.1,