rs121908941

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121908941(G;G)

Make rs121908941(G;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

32802416

Gene

DNMT3B

is a	snp
is	mentioned by
dbSNP	rs121908941
dbSNP (classic)	rs121908941
ClinGen	rs121908941
ebi	rs121908941
HLI	rs121908941
Exac	rs121908941
Gnomad	rs121908941
Varsome	rs121908941
LitVar	rs121908941
Map	rs121908941
PheGenI	rs121908941
Biobank	rs121908941
1000 genomes	rs121908941
hgdp	rs121908941
ensembl	rs121908941
geneview	rs121908941
scholar	rs121908941
google	rs121908941
pharmgkb	rs121908941
gwascentral	rs121908941
openSNP	rs121908941
23andMe	rs121908941
SNPshot	rs121908941
SNPdbe	rs121908941
MSV3d	rs121908941
GWAS Ctlg	rs121908941

Max Magnitude

0

OMIM	602900
Desc
Variant	0003
Related	also

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,