rs587777136
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs587777136(C;T) | 
| Make rs587777136(T;T) | 
| Reference | GRCh38 38.1/142 | 
| Chromosome | 17 | 
| Position | 42562797 | 
| Gene | COASY | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs587777136 | 
| dbSNP (classic) | rs587777136 | 
| ClinGen | rs587777136 | 
| ebi | rs587777136 | 
| HLI | rs587777136 | 
| Exac | rs587777136 | 
| Gnomad | rs587777136 | 
| Varsome | rs587777136 | 
| LitVar | rs587777136 | 
| Map | rs587777136 | 
| PheGenI | rs587777136 | 
| Biobank | rs587777136 | 
| 1000 genomes | rs587777136 | 
| hgdp | rs587777136 | 
| ensembl | rs587777136 | 
| geneview | rs587777136 | 
| scholar | rs587777136 | 
| rs587777136 | |
| pharmgkb | rs587777136 | 
| gwascentral | rs587777136 | 
| openSNP | rs587777136 | 
| 23andMe | rs587777136 | 
| SNPshot | rs587777136 | 
| SNPdbe | rs587777136 | 
| MSV3d | rs587777136 | 
| GWAS Ctlg | rs587777136 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs587777136(T;T) | 
| Alt | rs587777136(T;T) | 
| Reference | Rs587777136(C;C) | 
| Significance | Pathogenic | 
| Disease | Neurodegeneration with brain iron accumulation 6 | 
| Variation | info | 
| Gene | COASY | 
| CLNDBN | Neurodegeneration with brain iron accumulation 6 | 
| Reversed | 0 | 
| HGVS | NC_000017.10:g.40714815C>T | 
| CLNSRC | OMIM Allelic Variant | 
| CLNACC | RCV000087063.4, | 
