rs448740
From SNPedia
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 |
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, |