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rs786202840

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202840(G;T)
Make rs786202840(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960942
GenePTEN
is asnp
is mentioned by
dbSNPrs786202840
ebirs786202840
HLIrs786202840
Exacrs786202840
Varsomers786202840
Maprs786202840
PheGenIrs786202840
hapmaprs786202840
1000 genomesrs786202840
hgdprs786202840
ensemblrs786202840
gopubmedrs786202840
geneviewrs786202840
scholarrs786202840
googlers786202840
pharmgkbrs786202840
gwascentralrs786202840
openSNPrs786202840
23andMers786202840
23andMe allrs786202840
SNP Nexus

SNPshotrs786202840
SNPdbers786202840
MSV3drs786202840
GWAS Ctlgrs786202840
Max Magnitude0
ClinVar
Risk rs786202840(T;T)
Alt rs786202840(T;T)
Reference rs786202840(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720699G>T
CLNSRC
CLNACC RCV000165862.1,