rs587776807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587776807(-;T) |
Make rs587776807(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 159323098 |
Gene | IL12B, LOC107986469 |
is a | snp |
is | mentioned by |
dbSNP | rs587776807 |
dbSNP (classic) | rs587776807 |
ClinGen | rs587776807 |
ebi | rs587776807 |
HLI | rs587776807 |
Exac | rs587776807 |
Gnomad | rs587776807 |
Varsome | rs587776807 |
LitVar | rs587776807 |
Map | rs587776807 |
PheGenI | rs587776807 |
Biobank | rs587776807 |
1000 genomes | rs587776807 |
hgdp | rs587776807 |
ensembl | rs587776807 |
geneview | rs587776807 |
scholar | rs587776807 |
rs587776807 | |
pharmgkb | rs587776807 |
gwascentral | rs587776807 |
openSNP | rs587776807 |
23andMe | rs587776807 |
SNPshot | rs587776807 |
SNPdbe | rs587776807 |
MSV3d | rs587776807 |
GWAS Ctlg | rs587776807 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776807(T;T) |
Alt | rs587776807(T;T) |
Reference | Rs587776807(-;-) |
Significance | Pathogenic |
Disease | Immunodeficiency 29 |
Variation | info |
Gene | IL12B |
CLNDBN | Immunodeficiency 29 |
Reversed | 0 |
HGVS | NC_000005.9:g.158750106dupT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000015098.27, |