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rs786202529

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202529(-;-)
Make rs786202529(-;G)
Make rs786202529(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957924
GenePTEN
is asnp
is mentioned by
dbSNPrs786202529
ebirs786202529
HLIrs786202529
Exacrs786202529
Varsomers786202529
Maprs786202529
PheGenIrs786202529
hapmaprs786202529
1000 genomesrs786202529
hgdprs786202529
ensemblrs786202529
gopubmedrs786202529
geneviewrs786202529
scholarrs786202529
googlers786202529
pharmgkbrs786202529
gwascentralrs786202529
openSNPrs786202529
23andMers786202529
23andMe allrs786202529
SNP Nexus

SNPshotrs786202529
SNPdbers786202529
MSV3drs786202529
GWAS Ctlgrs786202529
Max Magnitude0
ClinVar
Risk rs786202529(G;G)
Alt rs786202529(G;G)
Reference rs786202529(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717681dupG
CLNSRC
CLNACC RCV000165377.1,