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rs786202733

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202733(C;G)
Make rs786202733(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952165
GenePTEN
is asnp
is mentioned by
dbSNPrs786202733
ebirs786202733
HLIrs786202733
Exacrs786202733
Varsomers786202733
Maprs786202733
PheGenIrs786202733
hapmaprs786202733
1000 genomesrs786202733
hgdprs786202733
ensemblrs786202733
gopubmedrs786202733
geneviewrs786202733
scholarrs786202733
googlers786202733
pharmgkbrs786202733
gwascentralrs786202733
openSNPrs786202733
23andMers786202733
23andMe allrs786202733
SNP Nexus

SNPshotrs786202733
SNPdbers786202733
MSV3drs786202733
GWAS Ctlgrs786202733
Max Magnitude0
ClinVar
Risk rs786202733(G;G)
Alt rs786202733(G;G)
Reference rs786202733(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711922C>G
CLNSRC
CLNACC RCV000165694.1,