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

rs121908939

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908939(A;G)
Make rs121908939(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position32807791
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs121908939
ClinGenrs121908939
ebirs121908939
HLIrs121908939
Exacrs121908939
Varsomers121908939
Maprs121908939
PheGenIrs121908939
hapmaprs121908939
1000 genomesrs121908939
hgdprs121908939
ensemblrs121908939
gopubmedrs121908939
geneviewrs121908939
scholarrs121908939
googlers121908939
pharmgkbrs121908939
gwascentralrs121908939
openSNPrs121908939
23andMers121908939
23andMe allrs121908939
SNP Nexus

SNPshotrs121908939
SNPdbers121908939
MSV3drs121908939
GWAS Ctlgrs121908939
Max Magnitude0
OMIM602900
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908939(G;G)
Alt rs121908939(G;G)
Reference Rs121908939(A;A)
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.31395597A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000007125.3,