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rs786204929

From SNPedia

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


Make rs786204929(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933144
GenePTEN
is asnp
is mentioned by
dbSNPrs786204929
ClinGenrs786204929
ebirs786204929
HLIrs786204929
Exacrs786204929
Varsomers786204929
Maprs786204929
PheGenIrs786204929
hapmaprs786204929
1000 genomesrs786204929
hgdprs786204929
ensemblrs786204929
gopubmedrs786204929
geneviewrs786204929
scholarrs786204929
googlers786204929
pharmgkbrs786204929
gwascentralrs786204929
openSNPrs786204929
23andMers786204929
23andMe allrs786204929
SNP Nexus

SNPshotrs786204929
SNPdbers786204929
MSV3drs786204929
GWAS Ctlgrs786204929
Max Magnitude6.3
ClinVar
Risk rs786204929(A;A)
Alt rs786204929(A;A)
Reference Rs786204929(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692901G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000169874.3,