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rs786204903

From SNPedia

Orientationplus
Geno Mag Summary
(ATCA;ATCA) 0 common in clinvar
Make rs786204903(-;-)
Make rs786204903(-;TCAA)
Make rs786204903(TCAA;TCAA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957976
GenePTEN
is asnp
is mentioned by
dbSNPrs786204903
ebirs786204903
HLIrs786204903
Exacrs786204903
Varsomers786204903
Maprs786204903
PheGenIrs786204903
hapmaprs786204903
1000 genomesrs786204903
hgdprs786204903
ensemblrs786204903
gopubmedrs786204903
geneviewrs786204903
scholarrs786204903
googlers786204903
pharmgkbrs786204903
gwascentralrs786204903
openSNPrs786204903
23andMers786204903
23andMe allrs786204903
SNP Nexus

SNPshotrs786204903
SNPdbers786204903
MSV3drs786204903
GWAS Ctlgrs786204903
Max Magnitude0
ClinVar
Risk rs786204903(;)
Alt rs786204903(;)
Reference rs786204903(ATCA;ATCA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717733_89717736delTCAA
CLNSRC
CLNACC RCV000169844.1,