rs966681982
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Reference | GRCh38.p7 38.3/150 | 
| Chromosome | 17 | 
| Position | 6703140 | 
| Gene | SLC13A5 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs966681982 | 
| dbSNP (classic) | rs966681982 | 
| ClinGen | rs966681982 | 
| ebi | rs966681982 | 
| HLI | rs966681982 | 
| Exac | rs966681982 | 
| Gnomad | rs966681982 | 
| Varsome | rs966681982 | 
| LitVar | rs966681982 | 
| Map | rs966681982 | 
| PheGenI | rs966681982 | 
| Biobank | rs966681982 | 
| 1000 genomes | rs966681982 | 
| hgdp | rs966681982 | 
| ensembl | rs966681982 | 
| geneview | rs966681982 | 
| scholar | rs966681982 | 
| rs966681982 | |
| pharmgkb | rs966681982 | 
| gwascentral | rs966681982 | 
| openSNP | rs966681982 | 
| 23andMe | rs966681982 | 
| SNPshot | rs966681982 | 
| SNPdbe | rs966681982 | 
| MSV3d | rs966681982 | 
| GWAS Ctlg | rs966681982 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs966681982(C;C) | 
| Alt | rs966681982(C;C) | 
| Reference | Rs966681982(T;T) | 
| Significance | Probable-Pathogenic | 
| Disease | not provided | 
| Variation | info | 
| Gene | |
| CLNDBN | not provided | 
| Reversed | 0 | 
| HGVS | NC_000017.10:g.6606459T>C | 
| CLNSRC | |
| CLNACC | RCV000485335.1, | 


