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rs796065342

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065342(C;T)
Make rs796065342(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position25246695
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs796065342
ebirs796065342
HLIrs796065342
Exacrs796065342
Varsomers796065342
Maprs796065342
PheGenIrs796065342
hapmaprs796065342
1000 genomesrs796065342
hgdprs796065342
ensemblrs796065342
gopubmedrs796065342
geneviewrs796065342
scholarrs796065342
googlers796065342
pharmgkbrs796065342
gwascentralrs796065342
openSNPrs796065342
23andMers796065342
23andMe allrs796065342
SNP Nexus

SNPshotrs796065342
SNPdbers796065342
MSV3drs796065342
GWAS Ctlgrs796065342
Max Magnitude0
ClinVar
Risk rs796065342(T;T)
Alt rs796065342(T;T)
Reference rs796065342(C;C)
Significance Pathogenic
Disease Early T cell progenitor acute lymphoblastic leukemia
Variation info
Gene DNMT3A
CLNDBN Early T cell progenitor acute lymphoblastic leukemia
Reversed 1
HGVS NC_000002.11:g.25469564G>A
CLNSRC
CLNACC RCV000190418.1,