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rs779626155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779626155(A;A)
Make rs779626155(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position25240313
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs779626155
dbSNP (classic)rs779626155
ClinGenrs779626155
ebirs779626155
HLIrs779626155
Exacrs779626155
Gnomadrs779626155
Varsomers779626155
LitVarrs779626155
Maprs779626155
PheGenIrs779626155
Biobankrs779626155
1000 genomesrs779626155
hgdprs779626155
ensemblrs779626155
geneviewrs779626155
scholarrs779626155
googlers779626155
pharmgkbrs779626155
gwascentralrs779626155
openSNPrs779626155
23andMers779626155
SNPshotrs779626155
SNPdbers779626155
MSV3drs779626155
GWAS Ctlgrs779626155
Max Magnitude0
ClinVar
Risk rs779626155(A;A)
Alt rs779626155(A;A)
Reference Rs779626155(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.25463182G>A
CLNSRC
CLNACC RCV000486209.1,