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rs786204906

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204906(-;-)
Make rs786204906(-;GTGCA)
Make rs786204906(GTGCA;GTGCA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87961020
GenePTEN
is asnp
is mentioned by
dbSNPrs786204906
ebirs786204906
HLIrs786204906
Exacrs786204906
Varsomers786204906
Maprs786204906
PheGenIrs786204906
hapmaprs786204906
1000 genomesrs786204906
hgdprs786204906
ensemblrs786204906
gopubmedrs786204906
geneviewrs786204906
scholarrs786204906
googlers786204906
pharmgkbrs786204906
gwascentralrs786204906
openSNPrs786204906
23andMers786204906
23andMe allrs786204906
SNP Nexus

SNPshotrs786204906
SNPdbers786204906
MSV3drs786204906
GWAS Ctlgrs786204906
Max Magnitude0
ClinVar
Risk rs786204906(GTGCA;GTGCA)
Alt rs786204906(GTGCA;GTGCA)
Reference rs786204906(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720777_89720778insGTGCA
CLNSRC
CLNACC RCV000169847.1,