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rs786203477

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203477(-;-)
Make rs786203477(-;CT)
Make rs786203477(CT;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894026
GenePTEN
is asnp
is mentioned by
dbSNPrs786203477
ebirs786203477
HLIrs786203477
Exacrs786203477
Varsomers786203477
Maprs786203477
PheGenIrs786203477
hapmaprs786203477
1000 genomesrs786203477
hgdprs786203477
ensemblrs786203477
gopubmedrs786203477
geneviewrs786203477
scholarrs786203477
googlers786203477
pharmgkbrs786203477
gwascentralrs786203477
openSNPrs786203477
23andMers786203477
23andMe allrs786203477
SNP Nexus

SNPshotrs786203477
SNPdbers786203477
MSV3drs786203477
GWAS Ctlgrs786203477
Max Magnitude0
ClinVar
Risk rs786203477(TC;TC)
Alt rs786203477(TC;TC)
Reference rs786203477(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653783_89653784insCT
CLNSRC
CLNACC RCV000166796.1,