rs1029273
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1029273(C;C) |
| Make rs1029273(C;T) |
| Make rs1029273(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 4675114 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1029273 |
| dbSNP (classic) | rs1029273 |
| ClinGen | rs1029273 |
| ebi | rs1029273 |
| HLI | rs1029273 |
| Exac | rs1029273 |
| Gnomad | rs1029273 |
| Varsome | rs1029273 |
| LitVar | rs1029273 |
| Map | rs1029273 |
| PheGenI | rs1029273 |
| Biobank | rs1029273 |
| 1000 genomes | rs1029273 |
| hgdp | rs1029273 |
| ensembl | rs1029273 |
| geneview | rs1029273 |
| scholar | rs1029273 |
| rs1029273 | |
| pharmgkb | rs1029273 |
| gwascentral | rs1029273 |
| openSNP | rs1029273 |
| 23andMe | rs1029273 |
| SNPshot | rs1029273 |
| SNPdbe | rs1029273 |
| MSV3d | rs1029273 |
| GWAS Ctlg | rs1029273 |
| GMAF | 0.4279 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 21616973] Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors
[PMID 19081515
] Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
