rs796051992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 3 | Carrier of a methylmalonic aciduria type cblA mutation |
| (C;C) | 0 | common in clinvar |
| Make rs796051992(A;A) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 145639526 |
| Gene | MMAA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs796051992 |
| dbSNP (classic) | rs796051992 |
| ClinGen | rs796051992 |
| ebi | rs796051992 |
| HLI | rs796051992 |
| Exac | rs796051992 |
| Gnomad | rs796051992 |
| Varsome | rs796051992 |
| LitVar | rs796051992 |
| Map | rs796051992 |
| PheGenI | rs796051992 |
| Biobank | rs796051992 |
| 1000 genomes | rs796051992 |
| hgdp | rs796051992 |
| ensembl | rs796051992 |
| geneview | rs796051992 |
| scholar | rs796051992 |
| rs796051992 | |
| pharmgkb | rs796051992 |
| gwascentral | rs796051992 |
| openSNP | rs796051992 |
| 23andMe | rs796051992 |
| SNPshot | rs796051992 |
| SNPdbe | rs796051992 |
| MSV3d | rs796051992 |
| GWAS Ctlg | rs796051992 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs796051992(A;A) |
| Alt | rs796051992(A;A) |
| Reference | Rs796051992(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MMAA |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.146560678C>A |
| CLNSRC | |
| CLNACC | RCV000186011.2, |
