rs373901523
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs373901523(G;T) |
| Make rs373901523(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 56887932 |
| Gene | SLC12A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs373901523 |
| dbSNP (classic) | rs373901523 |
| ClinGen | rs373901523 |
| ebi | rs373901523 |
| HLI | rs373901523 |
| Exac | rs373901523 |
| Gnomad | rs373901523 |
| Varsome | rs373901523 |
| LitVar | rs373901523 |
| Map | rs373901523 |
| PheGenI | rs373901523 |
| Biobank | rs373901523 |
| 1000 genomes | rs373901523 |
| hgdp | rs373901523 |
| ensembl | rs373901523 |
| geneview | rs373901523 |
| scholar | rs373901523 |
| rs373901523 | |
| pharmgkb | rs373901523 |
| gwascentral | rs373901523 |
| openSNP | rs373901523 |
| 23andMe | rs373901523 |
| SNPshot | rs373901523 |
| SNPdbe | rs373901523 |
| MSV3d | rs373901523 |
| GWAS Ctlg | rs373901523 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs373901523(A;A) rs373901523(T;T) |
| Alt | rs373901523(A;A) rs373901523(T;T) |
| Reference | Rs373901523(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SLC12A3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.56921844G>A |
| CLNSRC | |
| CLNACC | RCV000412838.1, |
