rs864321684
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs864321684(C;G) | 
| Make rs864321684(G;G) | 
| Reference | GRCh38.p2 38.2/146 | 
| Chromosome | 6 | 
| Position | 137877188 | 
| Gene | TNFAIP3 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs864321684 | 
| dbSNP (classic) | rs864321684 | 
| ClinGen | rs864321684 | 
| ebi | rs864321684 | 
| HLI | rs864321684 | 
| Exac | rs864321684 | 
| Gnomad | rs864321684 | 
| Varsome | rs864321684 | 
| LitVar | rs864321684 | 
| Map | rs864321684 | 
| PheGenI | rs864321684 | 
| Biobank | rs864321684 | 
| 1000 genomes | rs864321684 | 
| hgdp | rs864321684 | 
| ensembl | rs864321684 | 
| geneview | rs864321684 | 
| scholar | rs864321684 | 
| rs864321684 | |
| pharmgkb | rs864321684 | 
| gwascentral | rs864321684 | 
| openSNP | rs864321684 | 
| 23andMe | rs864321684 | 
| SNPshot | rs864321684 | 
| SNPdbe | rs864321684 | 
| MSV3d | rs864321684 | 
| GWAS Ctlg | rs864321684 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs864321684(G;G) | 
| Alt | rs864321684(G;G) | 
| Reference | Rs864321684(C;C) | 
| Significance | Pathogenic | 
| Disease | Autoinflammatory syndrome | 
| Variation | info | 
| Gene | TNFAIP3 | 
| CLNDBN | Autoinflammatory syndrome, familial, Behcet-like | 
| Reversed | 0 | 
| HGVS | NC_000006.11:g.138198325C>G | 
| CLNSRC | OMIM Allelic Variant | 
| CLNACC | RCV000203553.1, | 


