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rs377577594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377577594(A;A)
Make rs377577594(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position25234374
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs377577594
dbSNP (old)rs377577594
ClinGenrs377577594
ebirs377577594
HLIrs377577594
Exacrs377577594
Varsomers377577594
Maprs377577594
PheGenIrs377577594
Biobankrs377577594
1000 genomesrs377577594
hgdprs377577594
ensemblrs377577594
gopubmedrs377577594
geneviewrs377577594
scholarrs377577594
googlers377577594
pharmgkbrs377577594
gwascentralrs377577594
openSNPrs377577594
23andMers377577594
23andMe allrs377577594
SNP Nexus

SNPshotrs377577594
SNPdbers377577594
MSV3drs377577594
GWAS Ctlgrs377577594
Max Magnitude0
ClinVar
Risk rs377577594(A;A) rs377577594(C;C) rs377577594(T;T)
Alt rs377577594(A;A) rs377577594(C;C) rs377577594(T;T)
Reference Rs377577594(G;G)
Significance Pathogenic
Disease Myelodysplastic syndrome Acute myeloid leukemia Adenocarcinoma of lung
Variation info
Gene DNMT3A
CLNDBN Myelodysplastic syndrome Acute myeloid leukemia Adenocarcinoma of lung
Reversed 0
HGVS NC_000002.11:g.25457243G>A; NC_000002.11:g.25457243G>C; NC_000002.11:g.25457243G>T
CLNSRC
CLNACC RCV000422474.1, RCV000429128.1, RCV000439787.1, RCV000427931.1, RCV000438614.1,