rs190007694
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs190007694(G;G) |
| Make rs190007694(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 43946109 |
| Gene | LRPPRC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs190007694 |
| dbSNP (classic) | rs190007694 |
| ClinGen | rs190007694 |
| ebi | rs190007694 |
| HLI | rs190007694 |
| Exac | rs190007694 |
| Gnomad | rs190007694 |
| Varsome | rs190007694 |
| LitVar | rs190007694 |
| Map | rs190007694 |
| PheGenI | rs190007694 |
| Biobank | rs190007694 |
| 1000 genomes | rs190007694 |
| hgdp | rs190007694 |
| ensembl | rs190007694 |
| geneview | rs190007694 |
| scholar | rs190007694 |
| rs190007694 | |
| pharmgkb | rs190007694 |
| gwascentral | rs190007694 |
| openSNP | rs190007694 |
| 23andMe | rs190007694 |
| SNPshot | rs190007694 |
| SNPdbe | rs190007694 |
| MSV3d | rs190007694 |
| GWAS Ctlg | rs190007694 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs190007694(G;G) |
| Alt | rs190007694(G;G) |
| Reference | Rs190007694(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LRPPRC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.44173248T>G |
| CLNSRC | |
| CLNACC | RCV000199688.1, |
