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rs147001633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147001633(C;T)
Make rs147001633(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position25234373
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs147001633
dbSNP (old)rs147001633
ClinGenrs147001633
ebirs147001633
HLIrs147001633
Exacrs147001633
Varsomers147001633
Maprs147001633
PheGenIrs147001633
Biobankrs147001633
1000 genomesrs147001633
hgdprs147001633
ensemblrs147001633
gopubmedrs147001633
geneviewrs147001633
scholarrs147001633
googlers147001633
pharmgkbrs147001633
gwascentralrs147001633
openSNPrs147001633
23andMers147001633
23andMe allrs147001633
SNP Nexus

SNPshotrs147001633
SNPdbers147001633
MSV3drs147001633
GWAS Ctlgrs147001633
Max Magnitude0
ClinVar
Risk rs147001633(A;A) rs147001633(G;G) rs147001633(T;T)
Alt rs147001633(A;A) rs147001633(G;G) rs147001633(T;T)
Reference Rs147001633(C;C)
Significance Pathogenic
Disease Acute myeloid leukemia Adenocarcinoma of lung Myelodysplastic syndrome not provided
Variation info
Gene DNMT3A
CLNDBN Acute myeloid leukemia Adenocarcinoma of lung Myelodysplastic syndrome not provided
Reversed 0
HGVS NC_000002.11:g.25457242C>A; NC_000002.11:g.25457242C>G; NC_000002.11:g.25457242C>T
CLNSRC
CLNACC RCV000445240.1, RCV000419470.1, RCV000427788.1, RCV000436723.1, RCV000418424.1, RCV000430182.1, RCV000437399.1, RCV000485343.1,