rs121908939

Orientation

plus

Stabilized

plus

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

Make rs121908939(A;G)

Make rs121908939(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

32807791

Gene

DNMT3B

is a	snp
is	mentioned by
dbSNP	rs121908939
dbSNP (classic)	rs121908939
ClinGen	rs121908939
ebi	rs121908939
HLI	rs121908939
Exac	rs121908939
Gnomad	rs121908939
Varsome	rs121908939
LitVar	rs121908939
Map	rs121908939
PheGenI	rs121908939
Biobank	rs121908939
1000 genomes	rs121908939
hgdp	rs121908939
ensembl	rs121908939
geneview	rs121908939
scholar	rs121908939
google	rs121908939
pharmgkb	rs121908939
gwascentral	rs121908939
openSNP	rs121908939
23andMe	rs121908939
SNPshot	rs121908939
SNPdbe	rs121908939
MSV3d	rs121908939
GWAS Ctlg	rs121908939

Max Magnitude

0

OMIM	602900
Desc
Variant	0001
Related	also

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,