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rs786204866

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204866(A;G)
Make rs786204866(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952158
GenePTEN
is asnp
is mentioned by
dbSNPrs786204866
ebirs786204866
HLIrs786204866
Exacrs786204866
Varsomers786204866
Maprs786204866
PheGenIrs786204866
hapmaprs786204866
1000 genomesrs786204866
hgdprs786204866
ensemblrs786204866
gopubmedrs786204866
geneviewrs786204866
scholarrs786204866
googlers786204866
pharmgkbrs786204866
gwascentralrs786204866
openSNPrs786204866
23andMers786204866
23andMe allrs786204866
SNP Nexus

SNPshotrs786204866
SNPdbers786204866
MSV3drs786204866
GWAS Ctlgrs786204866
Max Magnitude0
ClinVar
Risk rs786204866(G;G)
Alt rs786204866(G;G)
Reference rs786204866(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.89711915A>G
CLNSRC
CLNACC RCV000169806.1,