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rs786204873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6.3 Hereditary cancer predisposing syndrome
(G;G) 0 common in clinvar


Make rs786204873(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87958020
GenePTEN
is asnp
is mentioned by
dbSNPrs786204873
dbSNP (old)rs786204873
ClinGenrs786204873
ebirs786204873
HLIrs786204873
Exacrs786204873
Gnomadrs786204873
Varsomers786204873
Maprs786204873
PheGenIrs786204873
Biobankrs786204873
1000 genomesrs786204873
hgdprs786204873
ensemblrs786204873
gopubmedrs786204873
geneviewrs786204873
scholarrs786204873
googlers786204873
pharmgkbrs786204873
gwascentralrs786204873
openSNPrs786204873
23andMers786204873
23andMe allrs786204873
SNP Nexus

SNPshotrs786204873
SNPdbers786204873
MSV3drs786204873
GWAS Ctlgrs786204873
Max Magnitude6.3
ClinVar
Risk rs786204873(A;A)
Alt rs786204873(A;A)
Reference Rs786204873(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89717777G>A
CLNSRC
CLNACC RCV000169813.2,