rs6638512
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6638512(C;C) |
Make rs6638512(C;T) |
Make rs6638512(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 5266661 |
is a | snp |
is | mentioned by |
dbSNP | rs6638512 |
dbSNP (classic) | rs6638512 |
ClinGen | rs6638512 |
ebi | rs6638512 |
HLI | rs6638512 |
Exac | rs6638512 |
Gnomad | rs6638512 |
Varsome | rs6638512 |
LitVar | rs6638512 |
Map | rs6638512 |
PheGenI | rs6638512 |
Biobank | rs6638512 |
1000 genomes | rs6638512 |
hgdp | rs6638512 |
ensembl | rs6638512 |
geneview | rs6638512 |
scholar | rs6638512 |
rs6638512 | |
pharmgkb | rs6638512 |
gwascentral | rs6638512 |
openSNP | rs6638512 |
23andMe | rs6638512 |
SNPshot | rs6638512 |
SNPdbe | rs6638512 |
MSV3d | rs6638512 |
GWAS Ctlg | rs6638512 |
GMAF | 0.4299 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22808956![]() |
Trait | Antineutrophil cytoplasmic antibody-associated vasculitis |
Title | Genetically distinct subsets within ANCA-associated vasculitis. |
Risk Allele | |
P-val | 2E-25 |
Odds Ratio | NR NR |