rs3771150
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3771150(C;C) |
Make rs3771150(C;T) |
Make rs3771150(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 102444391 |
Gene | IL18RAP |
is a | snp |
is | mentioned by |
dbSNP | rs3771150 |
dbSNP (classic) | rs3771150 |
ClinGen | rs3771150 |
ebi | rs3771150 |
HLI | rs3771150 |
Exac | rs3771150 |
Gnomad | rs3771150 |
Varsome | rs3771150 |
LitVar | rs3771150 |
Map | rs3771150 |
PheGenI | rs3771150 |
Biobank | rs3771150 |
1000 genomes | rs3771150 |
hgdp | rs3771150 |
ensembl | rs3771150 |
geneview | rs3771150 |
scholar | rs3771150 |
rs3771150 | |
pharmgkb | rs3771150 |
gwascentral | rs3771150 |
openSNP | rs3771150 |
23andMe | rs3771150 |
SNPshot | rs3771150 |
SNPdbe | rs3771150 |
MSV3d | rs3771150 |
GWAS Ctlg | rs3771150 |
GMAF | 0.2452 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]
[PMID 22289858] IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants