rs199890941
From SNPedia
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 |
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, |