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rs786204855

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204855(A;G)
Make rs786204855(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894084
GenePTEN
is asnp
is mentioned by
dbSNPrs786204855
ebirs786204855
HLIrs786204855
Exacrs786204855
Varsomers786204855
Maprs786204855
PheGenIrs786204855
hapmaprs786204855
1000 genomesrs786204855
hgdprs786204855
ensemblrs786204855
gopubmedrs786204855
geneviewrs786204855
scholarrs786204855
googlers786204855
pharmgkbrs786204855
gwascentralrs786204855
openSNPrs786204855
23andMers786204855
23andMe allrs786204855
SNP Nexus

SNPshotrs786204855
SNPdbers786204855
MSV3drs786204855
GWAS Ctlgrs786204855
Max Magnitude0
ClinVar
Risk rs786204855(G;G)
Alt rs786204855(G;G)
Reference rs786204855(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653841A>G
CLNSRC
CLNACC RCV000169790.1,