rs796051887
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs796051887(A;A) |
Make rs796051887(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 6021564 |
Gene | IL2RA |
is a | snp |
is | mentioned by |
dbSNP | rs796051887 |
dbSNP (classic) | rs796051887 |
ClinGen | rs796051887 |
ebi | rs796051887 |
HLI | rs796051887 |
Exac | rs796051887 |
Gnomad | rs796051887 |
Varsome | rs796051887 |
LitVar | rs796051887 |
Map | rs796051887 |
PheGenI | rs796051887 |
Biobank | rs796051887 |
1000 genomes | rs796051887 |
hgdp | rs796051887 |
ensembl | rs796051887 |
geneview | rs796051887 |
scholar | rs796051887 |
rs796051887 | |
pharmgkb | rs796051887 |
gwascentral | rs796051887 |
openSNP | rs796051887 |
23andMe | rs796051887 |
SNPshot | rs796051887 |
SNPdbe | rs796051887 |
MSV3d | rs796051887 |
GWAS Ctlg | rs796051887 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051887(A;A) |
Alt | rs796051887(A;A) |
Reference | Rs796051887(G;G) |
Significance | Pathogenic |
Disease | Interleukin 2 receptor |
Variation | info |
Gene | IL2RA |
CLNDBN | Interleukin 2 receptor, alpha, deficiency of |
Reversed | 1 |
HGVS | NC_000010.10:g.6063527C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000185641.3, |