rs199727887
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs199727887(G;G) |
| Make rs199727887(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 43977159 |
| Gene | LRPPRC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199727887 |
| dbSNP (classic) | rs199727887 |
| ClinGen | rs199727887 |
| ebi | rs199727887 |
| HLI | rs199727887 |
| Exac | rs199727887 |
| Gnomad | rs199727887 |
| Varsome | rs199727887 |
| LitVar | rs199727887 |
| Map | rs199727887 |
| PheGenI | rs199727887 |
| Biobank | rs199727887 |
| 1000 genomes | rs199727887 |
| hgdp | rs199727887 |
| ensembl | rs199727887 |
| geneview | rs199727887 |
| scholar | rs199727887 |
| rs199727887 | |
| pharmgkb | rs199727887 |
| gwascentral | rs199727887 |
| openSNP | rs199727887 |
| 23andMe | rs199727887 |
| SNPshot | rs199727887 |
| SNPdbe | rs199727887 |
| MSV3d | rs199727887 |
| GWAS Ctlg | rs199727887 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199727887(G;G) |
| Alt | rs199727887(G;G) |
| Reference | Rs199727887(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LRPPRC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.44204298T>G |
| CLNSRC | |
| CLNACC | RCV000198242.2, |
