rs121918126
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in clinvar | 
| Make rs121918126(C;C) | 
| Make rs121918126(C;G) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 16 | 
| Position | 55698005 | 
| Gene | SLC6A2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs121918126 | 
| dbSNP (classic) | rs121918126 | 
| ClinGen | rs121918126 | 
| ebi | rs121918126 | 
| HLI | rs121918126 | 
| Exac | rs121918126 | 
| Gnomad | rs121918126 | 
| Varsome | rs121918126 | 
| LitVar | rs121918126 | 
| Map | rs121918126 | 
| PheGenI | rs121918126 | 
| Biobank | rs121918126 | 
| 1000 genomes | rs121918126 | 
| hgdp | rs121918126 | 
| ensembl | rs121918126 | 
| geneview | rs121918126 | 
| scholar | rs121918126 | 
| rs121918126 | |
| pharmgkb | rs121918126 | 
| gwascentral | rs121918126 | 
| openSNP | rs121918126 | 
| 23andMe | rs121918126 | 
| SNPshot | rs121918126 | 
| SNPdbe | rs121918126 | 
| MSV3d | rs121918126 | 
| GWAS Ctlg | rs121918126 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs121918126(A;A) rs121918126(C;C) rs121918126(T;T) | 
| Alt | rs121918126(A;A) rs121918126(C;C) rs121918126(T;T) | 
| Reference | Rs121918126(G;G) | 
| Significance | Pathogenic | 
| Disease | Orthostatic intolerance | 
| Variation | info | 
| Gene | SLC6A2 | 
| CLNDBN | Orthostatic intolerance | 
| Reversed | 0 | 
| HGVS | NC_000016.9:g.55731917G>C | 
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) | 
| CLNACC | RCV000015043.25, | 


