rs35979293

Orientation

plus

Stabilized

plus

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

Make rs35979293(G;T)

Make rs35979293(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

28933379

Gene

CD19

is a	snp
is	mentioned by
dbSNP	rs35979293
dbSNP (classic)	rs35979293
ClinGen	rs35979293
ebi	rs35979293
HLI	rs35979293
Exac	rs35979293
Gnomad	rs35979293
Varsome	rs35979293
LitVar	rs35979293
Map	rs35979293
PheGenI	rs35979293
Biobank	rs35979293
1000 genomes	rs35979293
hgdp	rs35979293
ensembl	rs35979293
geneview	rs35979293
scholar	rs35979293
google	rs35979293
pharmgkb	rs35979293
gwascentral	rs35979293
openSNP	rs35979293
23andMe	rs35979293
SNPshot	rs35979293
SNPdbe	rs35979293
MSV3d	rs35979293
GWAS Ctlg	rs35979293

GMAF

0.2631

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis

ClinVar
Risk	rs35979293(A;A) rs35979293(T;T)
Alt	rs35979293(A;A) rs35979293(T;T)
Reference	Rs35979293(G;G)
Significance	Non-pathogenic
Disease	Common Variable Immune Deficiency
Variation	info
Gene	NPIPB8 CD19
CLNDBN	Common Variable Immune Deficiency, Recessive
Reversed	0
HGVS	NC_000016.9:g.28944700G>T
CLNSRC
CLNACC	RCV000271669.1,