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rs797044904

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044904(G;T)
Make rs797044904(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position25247713
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs797044904
ebirs797044904
HLIrs797044904
Exacrs797044904
Varsomers797044904
Maprs797044904
PheGenIrs797044904
hapmaprs797044904
1000 genomesrs797044904
hgdprs797044904
ensemblrs797044904
gopubmedrs797044904
geneviewrs797044904
scholarrs797044904
googlers797044904
pharmgkbrs797044904
gwascentralrs797044904
openSNPrs797044904
23andMers797044904
23andMe allrs797044904
SNP Nexus

SNPshotrs797044904
SNPdbers797044904
MSV3drs797044904
GWAS Ctlgrs797044904
Max Magnitude0
ClinVar
Risk rs797044904(T;T)
Alt rs797044904(T;T)
Reference rs797044904(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DNMT3A
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.25470582C>A
CLNSRC
CLNACC RCV000190731.1,