rs11078927
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11078927(C;C) |
Make rs11078927(C;T) |
Make rs11078927(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 39908152 |
Gene | GSDMB |
is a | snp |
is | mentioned by |
dbSNP | rs11078927 |
dbSNP (classic) | rs11078927 |
ClinGen | rs11078927 |
ebi | rs11078927 |
HLI | rs11078927 |
Exac | rs11078927 |
Gnomad | rs11078927 |
Varsome | rs11078927 |
LitVar | rs11078927 |
Map | rs11078927 |
PheGenI | rs11078927 |
Biobank | rs11078927 |
1000 genomes | rs11078927 |
hgdp | rs11078927 |
ensembl | rs11078927 |
geneview | rs11078927 |
scholar | rs11078927 |
rs11078927 | |
pharmgkb | rs11078927 |
gwascentral | rs11078927 |
openSNP | rs11078927 |
23andMe | rs11078927 |
SNPshot | rs11078927 |
SNPdbe | rs11078927 |
MSV3d | rs11078927 |
GWAS Ctlg | rs11078927 |
GMAF | 0.3269 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21804549] |
Trait | |
Title | Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. |
Risk Allele | |
P-val | 2E-16 |
Odds Ratio | None None |
[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.