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rs786204895

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204895(-;-)
Make rs786204895(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894062
GenePTEN
is asnp
is mentioned by
dbSNPrs786204895
ebirs786204895
HLIrs786204895
Exacrs786204895
Varsomers786204895
Maprs786204895
PheGenIrs786204895
hapmaprs786204895
1000 genomesrs786204895
hgdprs786204895
ensemblrs786204895
gopubmedrs786204895
geneviewrs786204895
scholarrs786204895
googlers786204895
pharmgkbrs786204895
gwascentralrs786204895
openSNPrs786204895
23andMers786204895
23andMe allrs786204895
SNP Nexus

SNPshotrs786204895
SNPdbers786204895
MSV3drs786204895
GWAS Ctlgrs786204895
Max Magnitude0
ClinVar
Risk rs786204895(;)
Alt rs786204895(;)
Reference rs786204895(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653819delA
CLNSRC
CLNACC RCV000169836.1,