rs770551610
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs770551610(G;T) |
Make rs770551610(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 50382603 |
Gene | IKZF1 |
is a | snp |
is | mentioned by |
dbSNP | rs770551610 |
dbSNP (classic) | rs770551610 |
ClinGen | rs770551610 |
ebi | rs770551610 |
HLI | rs770551610 |
Exac | rs770551610 |
Gnomad | rs770551610 |
Varsome | rs770551610 |
LitVar | rs770551610 |
Map | rs770551610 |
PheGenI | rs770551610 |
Biobank | rs770551610 |
1000 genomes | rs770551610 |
hgdp | rs770551610 |
ensembl | rs770551610 |
geneview | rs770551610 |
scholar | rs770551610 |
rs770551610 | |
pharmgkb | rs770551610 |
gwascentral | rs770551610 |
openSNP | rs770551610 |
23andMe | rs770551610 |
SNPshot | rs770551610 |
SNPdbe | rs770551610 |
MSV3d | rs770551610 |
GWAS Ctlg | rs770551610 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770551610(A;A) rs770551610(T;T) |
Alt | rs770551610(A;A) rs770551610(T;T) |
Reference | Rs770551610(G;G) |
Significance | Pathogenic |
Disease | Immunodeficiency |
Variation | info |
Gene | IKZF1 |
CLNDBN | Immunodeficiency, common variable, 13 |
Reversed | 0 |
HGVS | NC_000007.13:g.50450301G>A; NC_000007.13:g.50450301G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000210346.2, RCV000210351.2, |