rs448740

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	0.5	one of the differences in NA1 and NA2 neutrophil alloantigens
(T;T)	0	common in clinvar

Make rs448740(C;C)

Reference

GRCh38 38.1/142

Chromosome

1

Position

161629903

Gene

FCGR3B

is a	snp
is	mentioned by
dbSNP	rs448740
dbSNP (classic)	rs448740
ClinGen	rs448740
ebi	rs448740
HLI	rs448740
Exac	rs448740
Gnomad	rs448740
Varsome	rs448740
LitVar	rs448740
Map	rs448740
PheGenI	rs448740
Biobank	rs448740
1000 genomes	rs448740
hgdp	rs448740
ensembl	rs448740
geneview	rs448740
scholar	rs448740
google	rs448740
pharmgkb	rs448740
gwascentral	rs448740
openSNP	rs448740
23andMe	rs448740
SNPshot	rs448740
SNPdbe	rs448740
MSV3d	rs448740
GWAS Ctlg	rs448740

Merged from

Rs76714703

Max Magnitude

0.5

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs448740(C;C)
Alt	rs448740(C;C)
Reference	Rs448740(T;T)
Significance	Pathogenic
Disease	Neutrophil-specific antigens na1/na2
Variation	info
Gene	FCGR3B
CLNDBN	Neutrophil-specific antigens na1/na2
Reversed	0
HGVS	NC_000001.10:g.161599693T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030607.2,