rs2756271
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2756271(C;C) |
| Make rs2756271(C;T) |
| Make rs2756271(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 4684616 |
| Gene | PRNP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2756271 |
| dbSNP (classic) | rs2756271 |
| ClinGen | rs2756271 |
| ebi | rs2756271 |
| HLI | rs2756271 |
| Exac | rs2756271 |
| Gnomad | rs2756271 |
| Varsome | rs2756271 |
| LitVar | rs2756271 |
| Map | rs2756271 |
| PheGenI | rs2756271 |
| Biobank | rs2756271 |
| 1000 genomes | rs2756271 |
| hgdp | rs2756271 |
| ensembl | rs2756271 |
| geneview | rs2756271 |
| scholar | rs2756271 |
| rs2756271 | |
| pharmgkb | rs2756271 |
| gwascentral | rs2756271 |
| openSNP | rs2756271 |
| 23andMe | rs2756271 |
| SNPshot | rs2756271 |
| SNPdbe | rs2756271 |
| MSV3d | rs2756271 |
| GWAS Ctlg | rs2756271 |
| GMAF | 0.4123 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22561193
] Genotype patterns and characteristics of PRNP in the Korean population
[PMID 18347820] Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.
