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rs786201044

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201044(C;C)
Make rs786201044(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933165
GenePTEN
is asnp
is mentioned by
dbSNPrs786201044
ebirs786201044
HLIrs786201044
Exacrs786201044
Varsomers786201044
Maprs786201044
PheGenIrs786201044
hapmaprs786201044
1000 genomesrs786201044
hgdprs786201044
ensemblrs786201044
gopubmedrs786201044
geneviewrs786201044
scholarrs786201044
googlers786201044
pharmgkbrs786201044
gwascentralrs786201044
openSNPrs786201044
23andMers786201044
23andMe allrs786201044
SNP Nexus

SNPshotrs786201044
SNPdbers786201044
MSV3drs786201044
GWAS Ctlgrs786201044
Max Magnitude0
ClinVar
Risk rs786201044(C;C)
Alt rs786201044(C;C)
Reference rs786201044(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Acute megakaryoblastic leukemia Mediastinal germ cell tumor not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome Acute megakaryoblastic leukemia Mediastinal germ cell tumor not provided
Reversed 0
HGVS NC_000010.10:g.89692922T>C
CLNSRC
CLNACC RCV000162428.3, RCV000202582.1, RCV000212881.1,