rs148579886
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs148579886(A;A) |
| Make rs148579886(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 6 |
| Position | 39909922 |
| Gene | MOCS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148579886 |
| dbSNP (classic) | rs148579886 |
| ClinGen | rs148579886 |
| ebi | rs148579886 |
| HLI | rs148579886 |
| Exac | rs148579886 |
| Gnomad | rs148579886 |
| Varsome | rs148579886 |
| LitVar | rs148579886 |
| Map | rs148579886 |
| PheGenI | rs148579886 |
| Biobank | rs148579886 |
| 1000 genomes | rs148579886 |
| hgdp | rs148579886 |
| ensembl | rs148579886 |
| geneview | rs148579886 |
| scholar | rs148579886 |
| rs148579886 | |
| pharmgkb | rs148579886 |
| gwascentral | rs148579886 |
| openSNP | rs148579886 |
| 23andMe | rs148579886 |
| SNPshot | rs148579886 |
| SNPdbe | rs148579886 |
| MSV3d | rs148579886 |
| GWAS Ctlg | rs148579886 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs148579886(A;A) |
| Alt | rs148579886(A;A) |
| Reference | Rs148579886(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | Molybdenum cofactor deficiency not provided |
| Variation | info |
| Gene | MOCS1 |
| CLNDBN | Molybdenum cofactor deficiency, complementation group A not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.39877666G>A |
| CLNSRC | |
| CLNACC | RCV000190510.2, RCV000416188.1, |
