Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908947(C;C)
Make rs121908947(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32789007
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs121908947
ebirs121908947
HLIrs121908947
Exacrs121908947
Varsomers121908947
Maprs121908947
PheGenIrs121908947
hapmaprs121908947
1000 genomesrs121908947
hgdprs121908947
ensemblrs121908947
gopubmedrs121908947
geneviewrs121908947
scholarrs121908947
googlers121908947
pharmgkbrs121908947
gwascentralrs121908947
openSNPrs121908947
23andMers121908947
23andMe allrs121908947
SNP Nexus

SNPshotrs121908947
SNPdbers121908947
MSV3drs121908947
GWAS Ctlgrs121908947
Max Magnitude0
OMIM602900
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908947(C;C)
Alt rs121908947(C;C)
Reference rs121908947(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_000020.10:g.31376813T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007137.2,