rs864321626
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs864321626(C;T) |
Make rs864321626(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 137877081 |
Gene | TNFAIP3 |
is a | snp |
is | mentioned by |
dbSNP | rs864321626 |
dbSNP (classic) | rs864321626 |
ClinGen | rs864321626 |
ebi | rs864321626 |
HLI | rs864321626 |
Exac | rs864321626 |
Gnomad | rs864321626 |
Varsome | rs864321626 |
LitVar | rs864321626 |
Map | rs864321626 |
PheGenI | rs864321626 |
Biobank | rs864321626 |
1000 genomes | rs864321626 |
hgdp | rs864321626 |
ensembl | rs864321626 |
geneview | rs864321626 |
scholar | rs864321626 |
rs864321626 | |
pharmgkb | rs864321626 |
gwascentral | rs864321626 |
openSNP | rs864321626 |
23andMe | rs864321626 |
SNPshot | rs864321626 |
SNPdbe | rs864321626 |
MSV3d | rs864321626 |
GWAS Ctlg | rs864321626 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864321626(T;T) |
Alt | rs864321626(T;T) |
Reference | Rs864321626(C;C) |
Significance | Pathogenic |
Disease | Autoinflammatory syndrome |
Variation | info |
Gene | TNFAIP3 |
CLNDBN | Autoinflammatory syndrome, familial, Behcet-like |
Reversed | 0 |
HGVS | NC_000006.11:g.138198218C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000203503.2, |