rs199890941

Merged into

rs2290834

Orientation

plus

Stabilized

plus

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

Make rs199890941(C;C)

Make rs199890941(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161629781

Gene

FCGR3B

is a	snp
is	mentioned by
dbSNP	rs199890941
dbSNP (classic)	rs199890941
ClinGen	rs199890941
ebi	rs199890941
HLI	rs199890941
Exac	rs199890941
Gnomad	rs199890941
Varsome	rs199890941
LitVar	rs199890941
Map	rs199890941
PheGenI	rs199890941
Biobank	rs199890941
1000 genomes	rs199890941
hgdp	rs199890941
ensembl	rs199890941
geneview	rs199890941
scholar	rs199890941
google	rs199890941
pharmgkb	rs199890941
gwascentral	rs199890941
openSNP	rs199890941
23andMe	rs199890941
SNPshot	rs199890941
SNPdbe	rs199890941
MSV3d	rs199890941
GWAS Ctlg	rs199890941

Status

Merged into rs2290834

Max Magnitude

0

ClinVar
Risk	rs199890941(C;C)
Alt	rs199890941(C;C)
Reference	Rs199890941(T;T)
Significance	Pathogenic
Disease	Neutrophil-specific antigens na1/na2
Variation	info
Gene	FCGR3B
CLNDBN	Neutrophil-specific antigens na1/na2
Reversed	0
HGVS	NC_000001.11:g.161629781T\x3d
CLNSRC	ClinVar OMIM Allelic Variant
CLNACC	RCV000030607.1,