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rs786202688

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202688(A;G)
Make rs786202688(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933234
GenePTEN
is asnp
is mentioned by
dbSNPrs786202688
ebirs786202688
HLIrs786202688
Exacrs786202688
Varsomers786202688
Maprs786202688
PheGenIrs786202688
hapmaprs786202688
1000 genomesrs786202688
hgdprs786202688
ensemblrs786202688
gopubmedrs786202688
geneviewrs786202688
scholarrs786202688
googlers786202688
pharmgkbrs786202688
gwascentralrs786202688
openSNPrs786202688
23andMers786202688
23andMe allrs786202688
SNP Nexus

SNPshotrs786202688
SNPdbers786202688
MSV3drs786202688
GWAS Ctlgrs786202688
Max Magnitude0
ClinVar
Risk rs786202688(G;G)
Alt rs786202688(G;G)
Reference rs786202688(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692991A>G
CLNSRC
CLNACC RCV000165624.1,