rs587777338
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587777338(A;G) |
Make rs587777338(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 122620866 |
Gene | IL21, IL21-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs587777338 |
dbSNP (classic) | rs587777338 |
ClinGen | rs587777338 |
ebi | rs587777338 |
HLI | rs587777338 |
Exac | rs587777338 |
Gnomad | rs587777338 |
Varsome | rs587777338 |
LitVar | rs587777338 |
Map | rs587777338 |
PheGenI | rs587777338 |
Biobank | rs587777338 |
1000 genomes | rs587777338 |
hgdp | rs587777338 |
ensembl | rs587777338 |
geneview | rs587777338 |
scholar | rs587777338 |
rs587777338 | |
pharmgkb | rs587777338 |
gwascentral | rs587777338 |
openSNP | rs587777338 |
23andMe | rs587777338 |
SNPshot | rs587777338 |
SNPdbe | rs587777338 |
MSV3d | rs587777338 |
GWAS Ctlg | rs587777338 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777338(G;G) |
Alt | rs587777338(G;G) |
Reference | Rs587777338(A;A) |
Significance | Pathogenic |
Disease | Common variable immunodeficiency 11 |
Variation | info |
Gene | IL21 IL21-AS1 |
CLNDBN | Common variable immunodeficiency 11 |
Reversed | 0 |
HGVS | NC_000004.11:g.123542021A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000114995.6, |