rs11966200
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
(C;T) | 1.88x risk of vitiligo | |
(T;T) | 1.88x risk of vitiligo |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31869289 |
Gene | SLC44A4 |
is a | snp |
is | mentioned by |
dbSNP | rs11966200 |
dbSNP (classic) | rs11966200 |
ClinGen | rs11966200 |
ebi | rs11966200 |
HLI | rs11966200 |
Exac | rs11966200 |
Gnomad | rs11966200 |
Varsome | rs11966200 |
LitVar | rs11966200 |
Map | rs11966200 |
PheGenI | rs11966200 |
Biobank | rs11966200 |
1000 genomes | rs11966200 |
hgdp | rs11966200 |
ensembl | rs11966200 |
geneview | rs11966200 |
scholar | rs11966200 |
rs11966200 | |
pharmgkb | rs11966200 |
gwascentral | rs11966200 |
openSNP | rs11966200 |
23andMe | rs11966200 |
SNPshot | rs11966200 |
SNPdbe | rs11966200 |
MSV3d | rs11966200 |
GWAS Ctlg | rs11966200 |
GMAF | 0.04591 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20526339] |
Trait | Vitiligo |
Title | Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC |
Risk Allele | A |
P-val | 1E-48 |
Odds Ratio | 1.90 [1.74-2.07] |
[PMID 23516070] The association between a single nucleotide polymorphism rs11966200 in MHC region and clinical features of generalized vitiligo in Chinese Han population