rs6618677
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6618677(A;A) |
Make rs6618677(A;G) |
Make rs6618677(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 91557719 |
is a | snp |
is | mentioned by |
dbSNP | rs6618677 |
dbSNP (classic) | rs6618677 |
ClinGen | rs6618677 |
ebi | rs6618677 |
HLI | rs6618677 |
Exac | rs6618677 |
Gnomad | rs6618677 |
Varsome | rs6618677 |
LitVar | rs6618677 |
Map | rs6618677 |
PheGenI | rs6618677 |
Biobank | rs6618677 |
1000 genomes | rs6618677 |
hgdp | rs6618677 |
ensembl | rs6618677 |
geneview | rs6618677 |
scholar | rs6618677 |
rs6618677 | |
pharmgkb | rs6618677 |
gwascentral | rs6618677 |
openSNP | rs6618677 |
23andMe | rs6618677 |
SNPshot | rs6618677 |
SNPdbe | rs6618677 |
MSV3d | rs6618677 |
GWAS Ctlg | rs6618677 |
GMAF | 0.2388 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22808956] |
Trait | Antineutrophil cytoplasmic antibody-associated vasculitis |
Title | Genetically distinct subsets within ANCA-associated vasculitis. |
Risk Allele | |
P-val | 4E-8 |
Odds Ratio | 1.43 [NR] |