rs58599399
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs58599399(G;T) |
| Make rs58599399(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 49295621 |
| Gene | LOC101927267, PRPH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs58599399 |
| dbSNP (classic) | rs58599399 |
| ClinGen | rs58599399 |
| ebi | rs58599399 |
| HLI | rs58599399 |
| Exac | rs58599399 |
| Gnomad | rs58599399 |
| Varsome | rs58599399 |
| LitVar | rs58599399 |
| Map | rs58599399 |
| PheGenI | rs58599399 |
| Biobank | rs58599399 |
| 1000 genomes | rs58599399 |
| hgdp | rs58599399 |
| ensembl | rs58599399 |
| geneview | rs58599399 |
| scholar | rs58599399 |
| rs58599399 | |
| pharmgkb | rs58599399 |
| gwascentral | rs58599399 |
| openSNP | rs58599399 |
| 23andMe | rs58599399 |
| SNPshot | rs58599399 |
| SNPdbe | rs58599399 |
| MSV3d | rs58599399 |
| GWAS Ctlg | rs58599399 |
| GMAF | 0.001377 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs58599399(A;A) rs58599399(T;T) |
| Alt | rs58599399(A;A) rs58599399(T;T) |
| Reference | Rs58599399(G;G) |
| Significance | Other |
| Disease | Amyotrophic lateral sclerosis not provided |
| Variation | info |
| Gene | PRPH LOC101927267 RP11-161H23.9 |
| CLNDBN | Amyotrophic lateral sclerosis, susceptibility to not provided |
| Reversed | 0 |
| HGVS | NC_000012.11:g.49689404G>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000014706.2, RCV000057167.1, |
