rs200688856

Orientation

plus

Stabilized

plus

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

Make rs200688856(C;C)

Make rs200688856(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161629989

Gene

FCGR3B

is a	snp
is	mentioned by
dbSNP	rs200688856
dbSNP (classic)	rs200688856
ClinGen	rs200688856
ebi	rs200688856
HLI	rs200688856
Exac	rs200688856
Gnomad	rs200688856
Varsome	rs200688856
LitVar	rs200688856
Map	rs200688856
PheGenI	rs200688856
Biobank	rs200688856
1000 genomes	rs200688856
hgdp	rs200688856
ensembl	rs200688856
geneview	rs200688856
scholar	rs200688856
google	rs200688856
pharmgkb	rs200688856
gwascentral	rs200688856
openSNP	rs200688856
23andMe	rs200688856
SNPshot	rs200688856
SNPdbe	rs200688856
MSV3d	rs200688856
GWAS Ctlg	rs200688856

Max Magnitude

0

ClinVar
Risk	rs200688856(A;A) rs200688856(C;C)
Alt	rs200688856(A;A) rs200688856(C;C)
Reference	Rs200688856(G;G)
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.161599779G\x3d
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030607.2,