rs937746465
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 35860850 |
Gene | IL7R, LOC105374724 |
is a | snp |
is | mentioned by |
dbSNP | rs937746465 |
dbSNP (classic) | rs937746465 |
ClinGen | rs937746465 |
ebi | rs937746465 |
HLI | rs937746465 |
Exac | rs937746465 |
Gnomad | rs937746465 |
Varsome | rs937746465 |
LitVar | rs937746465 |
Map | rs937746465 |
PheGenI | rs937746465 |
Biobank | rs937746465 |
1000 genomes | rs937746465 |
hgdp | rs937746465 |
ensembl | rs937746465 |
geneview | rs937746465 |
scholar | rs937746465 |
rs937746465 | |
pharmgkb | rs937746465 |
gwascentral | rs937746465 |
openSNP | rs937746465 |
23andMe | rs937746465 |
SNPshot | rs937746465 |
SNPdbe | rs937746465 |
MSV3d | rs937746465 |
GWAS Ctlg | rs937746465 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs937746465(T;T) |
Alt | rs937746465(T;T) |
Reference | Rs937746465(A;A) |
Significance | Pathogenic |
Disease | Severe Combined Immune Deficiency not provided |
Variation | info |
Gene | |
CLNDBN | Severe Combined Immune Deficiency not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.35860952A>T |
CLNSRC | |
CLNACC | RCV000341907.1, RCV000485322.1, |