rs121918282
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs121918282(C;C) |
| Make rs121918282(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 123653773 |
| Gene | LOC105369543, SCN3B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121918282 |
| dbSNP (classic) | rs121918282 |
| ClinGen | rs121918282 |
| ebi | rs121918282 |
| HLI | rs121918282 |
| Exac | rs121918282 |
| Gnomad | rs121918282 |
| Varsome | rs121918282 |
| LitVar | rs121918282 |
| Map | rs121918282 |
| PheGenI | rs121918282 |
| Biobank | rs121918282 |
| 1000 genomes | rs121918282 |
| hgdp | rs121918282 |
| ensembl | rs121918282 |
| geneview | rs121918282 |
| scholar | rs121918282 |
| rs121918282 | |
| pharmgkb | rs121918282 |
| gwascentral | rs121918282 |
| openSNP | rs121918282 |
| 23andMe | rs121918282 |
| SNPshot | rs121918282 |
| SNPdbe | rs121918282 |
| MSV3d | rs121918282 |
| GWAS Ctlg | rs121918282 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121918282(C;C) |
| Alt | rs121918282(C;C) |
| Reference | Rs121918282(T;T) |
| Significance | Other |
| Disease | Brugada syndrome 7 Atrial fibrillation not provided Brugada syndrome not specified Cardiovascular phenotype |
| Variation | info |
| Gene | SCN3B |
| CLNDBN | Brugada syndrome 7 Atrial fibrillation, familial, 16 not provided Brugada syndrome not specified Cardiovascular phenotype |
| Reversed | 1 |
| HGVS | NC_000011.9:g.123524481A>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000002574.9, RCV000128811.6, RCV000171069.4, RCV000171567.2, RCV000220802.1, RCV000250087.1, |
[PMID 32354559] Association of Genetic Polymorphisms of TGF-β1, HMOX1, and APOL1 With CKD in Nigerian Patients With and Without HIV.
