rs267606711

Orientation

minus

Stabilized

minus

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

Make rs267606711(C;T)

Make rs267606711(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

63930266

Gene

CD79B

is a	snp
is	mentioned by
dbSNP	rs267606711
dbSNP (classic)	rs267606711
ClinGen	rs267606711
ebi	rs267606711
HLI	rs267606711
Exac	rs267606711
Gnomad	rs267606711
Varsome	rs267606711
LitVar	rs267606711
Map	rs267606711
PheGenI	rs267606711
Biobank	rs267606711
1000 genomes	rs267606711
hgdp	rs267606711
ensembl	rs267606711
geneview	rs267606711
scholar	rs267606711
google	rs267606711
pharmgkb	rs267606711
gwascentral	rs267606711
openSNP	rs267606711
23andMe	rs267606711
SNPshot	rs267606711
SNPdbe	rs267606711
MSV3d	rs267606711
GWAS Ctlg	rs267606711

Max Magnitude

0

ClinVar
Risk	rs267606711(T;T)
Alt	rs267606711(T;T)
Reference	Rs267606711(C;C)
Significance	Pathogenic
Disease	Agammaglobulinemia 6
Variation	info
Gene	CD79B
CLNDBN	Agammaglobulinemia 6, autosomal recessive
Reversed	1
HGVS	NC_000017.10:g.62007626G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015926.22,