rs569108
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(C;C) | ? | |
(C;T) | 3x risk of predisposition to childhood asthma in a Japanese population | |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 60095631 |
Gene | MS4A2 |
is a | snp |
is | mentioned by |
dbSNP | rs569108 |
dbSNP (classic) | rs569108 |
ClinGen | rs569108 |
ebi | rs569108 |
HLI | rs569108 |
Exac | rs569108 |
Gnomad | rs569108 |
Varsome | rs569108 |
LitVar | rs569108 |
Map | rs569108 |
PheGenI | rs569108 |
Biobank | rs569108 |
1000 genomes | rs569108 |
hgdp | rs569108 |
ensembl | rs569108 |
geneview | rs569108 |
scholar | rs569108 |
rs569108 | |
pharmgkb | rs569108 |
gwascentral | rs569108 |
openSNP | rs569108 |
23andMe | rs569108 |
SNPshot | rs569108 |
SNPdbe | rs569108 |
MSV3d | rs569108 |
GWAS Ctlg | rs569108 |
GMAF | 0.1194 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs569108, a SNP in the MS4A2 gene, has been linked in a Japanese population to a predisposition to childhood asthma, with an odds ratio of 3 [PMID 8842731, PMID 8968765]. The risk allele in dbSNP orientation is (C). [Note: no (C;C) homozygotes were observed in this population.]
ClinVar | |
---|---|
Risk | Rs569108(C;C) |
Alt | Rs569108(C;C) |
Reference | Rs569108(T;T) |
Significance | Other |
Disease | Atopic asthma |
Variation | info |
Gene | MS4A2 |
CLNDBN | Atopic asthma, susceptibility to |
Reversed | 1 |
HGVS | NC_000011.9:g.59863104A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015930.3, |
[PMID 15726497] Gene-environment interaction effects on the development of immune responses in the 1st year of life.
[PMID 16519819] Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19330901] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
[PMID 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 27746735] FCERI and Histamine Metabolism Gene Variability in Selective Responders to NSAIDS.
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
- Pages using PMID magic links