rs291102
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs291102(C;T) |
| Make rs291102(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 206933133 |
| Gene | PIGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs291102 |
| dbSNP (classic) | rs291102 |
| ClinGen | rs291102 |
| ebi | rs291102 |
| HLI | rs291102 |
| Exac | rs291102 |
| Gnomad | rs291102 |
| Varsome | rs291102 |
| LitVar | rs291102 |
| Map | rs291102 |
| PheGenI | rs291102 |
| Biobank | rs291102 |
| 1000 genomes | rs291102 |
| hgdp | rs291102 |
| ensembl | rs291102 |
| geneview | rs291102 |
| scholar | rs291102 |
| rs291102 | |
| pharmgkb | rs291102 |
| gwascentral | rs291102 |
| openSNP | rs291102 |
| 23andMe | rs291102 |
| SNPshot | rs291102 |
| SNPdbe | rs291102 |
| MSV3d | rs291102 |
| GWAS Ctlg | rs291102 |
| GMAF | 0.2296 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs291102(T;T) |
| Alt | rs291102(T;T) |
| Reference | Rs291102(C;C) |
| Significance | Unknown |
| Disease | Berger disease |
| Variation | info |
| Gene | PIGR |
| CLNDBN | Berger disease |
| Reversed | 1 |
| HGVS | NC_000001.10:g.207106478G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000014481.2, |
