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rs121908942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908942(A;A)
Make rs121908942(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position32800916
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs121908942
ebirs121908942
HLIrs121908942
Exacrs121908942
Varsomers121908942
Maprs121908942
PheGenIrs121908942
hapmaprs121908942
1000 genomesrs121908942
hgdprs121908942
ensemblrs121908942
gopubmedrs121908942
geneviewrs121908942
scholarrs121908942
googlers121908942
pharmgkbrs121908942
gwascentralrs121908942
openSNPrs121908942
23andMers121908942
23andMe allrs121908942
SNP Nexus

SNPshotrs121908942
SNPdbers121908942
MSV3drs121908942
GWAS Ctlgrs121908942
Max Magnitude0
OMIM602900
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908942(A;A)
Alt rs121908942(A;A)
Reference rs121908942(G;G)
Significance 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.31388722G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007128.4,