rs147574249
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs147574249(C;C) |
Make rs147574249(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 161629853 |
Gene | FCGR3B |
is a | snp |
is | mentioned by |
dbSNP | rs147574249 |
dbSNP (classic) | rs147574249 |
ClinGen | rs147574249 |
ebi | rs147574249 |
HLI | rs147574249 |
Exac | rs147574249 |
Gnomad | rs147574249 |
Varsome | rs147574249 |
LitVar | rs147574249 |
Map | rs147574249 |
PheGenI | rs147574249 |
Biobank | rs147574249 |
1000 genomes | rs147574249 |
hgdp | rs147574249 |
ensembl | rs147574249 |
geneview | rs147574249 |
scholar | rs147574249 |
rs147574249 | |
pharmgkb | rs147574249 |
gwascentral | rs147574249 |
openSNP | rs147574249 |
23andMe | rs147574249 |
SNPshot | rs147574249 |
SNPdbe | rs147574249 |
MSV3d | rs147574249 |
GWAS Ctlg | rs147574249 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147574249(C;C) |
Alt | rs147574249(C;C) |
Reference | Rs147574249(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.161599643T\x3d |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000030607.2, |