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rs786202918

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202918(C;T)
Make rs786202918(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957951
GenePTEN
is asnp
is mentioned by
dbSNPrs786202918
ebirs786202918
HLIrs786202918
Exacrs786202918
Varsomers786202918
Maprs786202918
PheGenIrs786202918
hapmaprs786202918
1000 genomesrs786202918
hgdprs786202918
ensemblrs786202918
gopubmedrs786202918
geneviewrs786202918
scholarrs786202918
googlers786202918
pharmgkbrs786202918
gwascentralrs786202918
openSNPrs786202918
23andMers786202918
23andMe allrs786202918
SNP Nexus

SNPshotrs786202918
SNPdbers786202918
MSV3drs786202918
GWAS Ctlgrs786202918
Max Magnitude0
ClinVar
Risk rs786202918(T;T)
Alt rs786202918(T;T)
Reference rs786202918(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.89717708C>T
CLNSRC
CLNACC RCV000165985.1,