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rs786203847

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203847(A;A)
Make rs786203847(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87925512
GenePTEN
is asnp
is mentioned by
dbSNPrs786203847
ebirs786203847
HLIrs786203847
Exacrs786203847
Varsomers786203847
Maprs786203847
PheGenIrs786203847
hapmaprs786203847
1000 genomesrs786203847
hgdprs786203847
ensemblrs786203847
gopubmedrs786203847
geneviewrs786203847
scholarrs786203847
googlers786203847
pharmgkbrs786203847
gwascentralrs786203847
openSNPrs786203847
23andMers786203847
23andMe allrs786203847
SNP Nexus

SNPshotrs786203847
SNPdbers786203847
MSV3drs786203847
GWAS Ctlgrs786203847
Max Magnitude0
ClinVar
Risk rs786203847(A;A)
Alt rs786203847(A;A)
Reference rs786203847(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89685269G>A
CLNSRC
CLNACC RCV000167333.3, RCV000212879.1,