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rs786204898

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204898(-;-)
Make rs786204898(-;AAGA)
Make rs786204898(AAGA;AAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87931058
GenePTEN
is asnp
is mentioned by
dbSNPrs786204898
ebirs786204898
HLIrs786204898
Exacrs786204898
Varsomers786204898
Maprs786204898
PheGenIrs786204898
hapmaprs786204898
1000 genomesrs786204898
hgdprs786204898
ensemblrs786204898
gopubmedrs786204898
geneviewrs786204898
scholarrs786204898
googlers786204898
pharmgkbrs786204898
gwascentralrs786204898
openSNPrs786204898
23andMers786204898
23andMe allrs786204898
SNP Nexus

SNPshotrs786204898
SNPdbers786204898
MSV3drs786204898
GWAS Ctlgrs786204898
Max Magnitude0
ClinVar
Risk rs786204898(GAAA;GAAA)
Alt rs786204898(GAAA;GAAA)
Reference rs786204898(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89690812_89690815dupAAGA
CLNSRC
CLNACC RCV000169839.1,