rs376993881
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs376993881(A;A) |
| Make rs376993881(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 80275073 |
| Gene | MAT1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs376993881 |
| dbSNP (classic) | rs376993881 |
| ClinGen | rs376993881 |
| ebi | rs376993881 |
| HLI | rs376993881 |
| Exac | rs376993881 |
| Gnomad | rs376993881 |
| Varsome | rs376993881 |
| LitVar | rs376993881 |
| Map | rs376993881 |
| PheGenI | rs376993881 |
| Biobank | rs376993881 |
| 1000 genomes | rs376993881 |
| hgdp | rs376993881 |
| ensembl | rs376993881 |
| geneview | rs376993881 |
| scholar | rs376993881 |
| rs376993881 | |
| pharmgkb | rs376993881 |
| gwascentral | rs376993881 |
| openSNP | rs376993881 |
| 23andMe | rs376993881 |
| SNPshot | rs376993881 |
| SNPdbe | rs376993881 |
| MSV3d | rs376993881 |
| GWAS Ctlg | rs376993881 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs376993881(A;A) |
| Alt | rs376993881(A;A) |
| Reference | Rs376993881(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MAT1A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.82034829G>A |
| CLNSRC | |
| CLNACC | RCV000481494.1, |
