rs2977838
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 0 | common in clinvar |
| Make rs2977838(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 144415027 |
| Gene | SLC39A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2977838 |
| dbSNP (classic) | rs2977838 |
| ClinGen | rs2977838 |
| ebi | rs2977838 |
| HLI | rs2977838 |
| Exac | rs2977838 |
| Gnomad | rs2977838 |
| Varsome | rs2977838 |
| LitVar | rs2977838 |
| Map | rs2977838 |
| PheGenI | rs2977838 |
| Biobank | rs2977838 |
| 1000 genomes | rs2977838 |
| hgdp | rs2977838 |
| ensembl | rs2977838 |
| geneview | rs2977838 |
| scholar | rs2977838 |
| rs2977838 | |
| pharmgkb | rs2977838 |
| gwascentral | rs2977838 |
| openSNP | rs2977838 |
| 23andMe | rs2977838 |
| SNPshot | rs2977838 |
| SNPdbe | rs2977838 |
| MSV3d | rs2977838 |
| GWAS Ctlg | rs2977838 |
| GMAF | 0.03535 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | Rs2977838(C;C) |
| Alt | Rs2977838(C;C) |
| Reference | Rs2977838(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | SLC39A4 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000008.10:g.145640411A>G |
| CLNSRC | |
| CLNACC | RCV000455209.1, |
