rs987106
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs987106(A;A) |
Make rs987106(A;T) |
Make rs987106(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 35875491 |
Gene | IL7R |
is a | snp |
is | mentioned by |
dbSNP | rs987106 |
dbSNP (classic) | rs987106 |
ClinGen | rs987106 |
ebi | rs987106 |
HLI | rs987106 |
Exac | rs987106 |
Gnomad | rs987106 |
Varsome | rs987106 |
LitVar | rs987106 |
Map | rs987106 |
PheGenI | rs987106 |
Biobank | rs987106 |
1000 genomes | rs987106 |
hgdp | rs987106 |
ensembl | rs987106 |
geneview | rs987106 |
scholar | rs987106 |
rs987106 | |
pharmgkb | rs987106 |
gwascentral | rs987106 |
openSNP | rs987106 |
23andMe | rs987106 |
SNPshot | rs987106 |
SNPdbe | rs987106 |
MSV3d | rs987106 |
GWAS Ctlg | rs987106 |
GMAF | 0.4601 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
Rs987106 | |
---|---|
PubMed | [PMID 17660816] |
Affy Probeset | SNP_A-4264835 |
Affy Orientation | same |
On GW 5.0 | 1 |
Alleles A/B | A/T |
Ancestral | T |
Population | |
Allele | T |
Case Freq. | |
Control Freq. | |
Odds Ratio Het | 0.79 |
Odds Ratio Hom | 1.26 |
Odds Ratio All | |
Disease | Multiple sclerosis (MS) |
rs987106 increases susceptibility to Multiple sclerosis 0.79 times for heterozygotes (AT) and 1.26 times for homozygotes (TT) [PMID 17660816]
[PMID 22329520] Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohort
[PMID 18563381] Study of the association between the CAPSL-IL7R locus and type 1 diabetes.