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rs2424932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2424932(A;G)
Make rs2424932(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position32808730
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs2424932
dbSNP (old)rs2424932
ClinGenrs2424932
ebirs2424932
HLIrs2424932
Exacrs2424932
Varsomers2424932
Maprs2424932
PheGenIrs2424932
Biobankrs2424932
1000 genomesrs2424932
hgdprs2424932
ensemblrs2424932
gopubmedrs2424932
geneviewrs2424932
scholarrs2424932
googlers2424932
pharmgkbrs2424932
gwascentralrs2424932
openSNPrs2424932
23andMers2424932
23andMe allrs2424932
SNP Nexus

SNPshotrs2424932
SNPdbers2424932
MSV3drs2424932
GWAS Ctlgrs2424932
GMAF0.2185
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 23025623] Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patients


[PMID 23666104OA-icon.png] DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population


[PMID 22382075OA-icon.png] Low-level environmental cadmium exposure is associated with DNA hypomethylation in Argentinean women.


[PMID 25038421] DNA methyltransferase haplotype is associated with Alzheimer's disease


ClinVar
Risk rs2424932(G;G) rs2424932(T;T)
Alt rs2424932(G;G) rs2424932(T;T)
Reference Rs2424932(A;A)
Significance Non-pathogenic
Disease Centromeric instability of chromosomes 1
Variation info
Gene DNMT3B
CLNDBN Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
Reversed 0
HGVS NC_000020.10:g.31396536A>G
CLNSRC
CLNACC RCV000368232.1,