rs76714703

Merged into

rs448740

Orientation

plus

Stabilized

plus

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

Make rs76714703(C;C)

Make rs76714703(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161629903

Gene

FCGR3B

is a	snp
is	mentioned by
dbSNP	rs76714703
dbSNP (classic)	rs76714703
ClinGen	rs76714703
ebi	rs76714703
HLI	rs76714703
Exac	rs76714703
Gnomad	rs76714703
Varsome	rs76714703
LitVar	rs76714703
Map	rs76714703
PheGenI	rs76714703
Biobank	rs76714703
1000 genomes	rs76714703
hgdp	rs76714703
ensembl	rs76714703
geneview	rs76714703
scholar	rs76714703
google	rs76714703
pharmgkb	rs76714703
gwascentral	rs76714703
openSNP	rs76714703
23andMe	rs76714703
SNPshot	rs76714703
SNPdbe	rs76714703
MSV3d	rs76714703
GWAS Ctlg	rs76714703

Status

Merged into rs448740

Max Magnitude

0

ClinVar
Risk	rs76714703(C;C)
Alt	rs76714703(C;C)
Reference	Rs76714703(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.161629903T>C
CLNSRC	ClinVar OMIM Allelic Variant
CLNACC	RCV000030607.1,