rs886041037
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 10 |
Position | 6024310 |
Gene | IL2RA |
is a | snp |
is | mentioned by |
dbSNP | rs886041037 |
dbSNP (classic) | rs886041037 |
ClinGen | rs886041037 |
ebi | rs886041037 |
HLI | rs886041037 |
Exac | rs886041037 |
Gnomad | rs886041037 |
Varsome | rs886041037 |
LitVar | rs886041037 |
Map | rs886041037 |
PheGenI | rs886041037 |
Biobank | rs886041037 |
1000 genomes | rs886041037 |
hgdp | rs886041037 |
ensembl | rs886041037 |
geneview | rs886041037 |
scholar | rs886041037 |
rs886041037 | |
pharmgkb | rs886041037 |
gwascentral | rs886041037 |
openSNP | rs886041037 |
23andMe | rs886041037 |
SNPshot | rs886041037 |
SNPdbe | rs886041037 |
MSV3d | rs886041037 |
GWAS Ctlg | rs886041037 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041037(T;T) |
Alt | rs886041037(T;T) |
Reference | Rs886041037(C;C) |
Significance | Pathogenic |
Disease | Interleukin 2 receptor |
Variation | info |
Gene | IL2RA |
CLNDBN | Interleukin 2 receptor, alpha, deficiency of |
Reversed | 1 |
HGVS | NC_000010.10:g.6066273G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000185639.3, |