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rs121908941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908941(G;G)
Make rs121908941(G;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32802416
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs121908941
ebirs121908941
HLIrs121908941
Exacrs121908941
Varsomers121908941
Maprs121908941
PheGenIrs121908941
hapmaprs121908941
1000 genomesrs121908941
hgdprs121908941
ensemblrs121908941
gopubmedrs121908941
geneviewrs121908941
scholarrs121908941
googlers121908941
pharmgkbrs121908941
gwascentralrs121908941
openSNPrs121908941
23andMers121908941
23andMe allrs121908941
SNP Nexus

SNPshotrs121908941
SNPdbers121908941
MSV3drs121908941
GWAS Ctlgrs121908941
Max Magnitude0
OMIM602900
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908941(G;G)
Alt rs121908941(G;G)
Reference rs121908941(T;T)
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_000020.11:g.32802416T>G
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000007127.1,