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rs786204904

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs786204904(-;-)
Make rs786204904(-;CT)
Make rs786204904(CT;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957989
GenePTEN
is asnp
is mentioned by
dbSNPrs786204904
ebirs786204904
HLIrs786204904
Exacrs786204904
Varsomers786204904
Maprs786204904
PheGenIrs786204904
hapmaprs786204904
1000 genomesrs786204904
hgdprs786204904
ensemblrs786204904
gopubmedrs786204904
geneviewrs786204904
scholarrs786204904
googlers786204904
pharmgkbrs786204904
gwascentralrs786204904
openSNPrs786204904
23andMers786204904
23andMe allrs786204904
SNP Nexus

SNPshotrs786204904
SNPdbers786204904
MSV3drs786204904
GWAS Ctlgrs786204904
Max Magnitude0
ClinVar
Risk rs786204904(;)
Alt rs786204904(;)
Reference rs786204904(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717746_89717747delCT
CLNSRC
CLNACC RCV000169845.1,