rs864621969
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs864621969(C;G) |
| Make rs864621969(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 9 |
| Position | 126615549 |
| Gene | LMX1B, LOC105376277 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs864621969 |
| dbSNP (classic) | rs864621969 |
| ClinGen | rs864621969 |
| ebi | rs864621969 |
| HLI | rs864621969 |
| Exac | rs864621969 |
| Gnomad | rs864621969 |
| Varsome | rs864621969 |
| LitVar | rs864621969 |
| Map | rs864621969 |
| PheGenI | rs864621969 |
| Biobank | rs864621969 |
| 1000 genomes | rs864621969 |
| hgdp | rs864621969 |
| ensembl | rs864621969 |
| geneview | rs864621969 |
| scholar | rs864621969 |
| rs864621969 | |
| pharmgkb | rs864621969 |
| gwascentral | rs864621969 |
| openSNP | rs864621969 |
| 23andMe | rs864621969 |
| SNPshot | rs864621969 |
| SNPdbe | rs864621969 |
| MSV3d | rs864621969 |
| GWAS Ctlg | rs864621969 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs864621969(G;G) |
| Alt | rs864621969(G;G) |
| Reference | Rs864621969(C;C) |
| Significance | Pathogenic |
| Disease | Nail-patella syndrome |
| Variation | info |
| Gene | LMX1B |
| CLNDBN | Nail-patella syndrome |
| Reversed | 0 |
| HGVS | NC_000009.11:g.129377828C>G |
| CLNSRC | |
| CLNACC | RCV000205274.1, |
