rs1048609704
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 130980606 |
| Gene | ATP2C1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048609704 |
| dbSNP (classic) | rs1048609704 |
| ClinGen | rs1048609704 |
| ebi | rs1048609704 |
| HLI | rs1048609704 |
| Exac | rs1048609704 |
| Gnomad | rs1048609704 |
| Varsome | rs1048609704 |
| LitVar | rs1048609704 |
| Map | rs1048609704 |
| PheGenI | rs1048609704 |
| Biobank | rs1048609704 |
| 1000 genomes | rs1048609704 |
| hgdp | rs1048609704 |
| ensembl | rs1048609704 |
| geneview | rs1048609704 |
| scholar | rs1048609704 |
| rs1048609704 | |
| pharmgkb | rs1048609704 |
| gwascentral | rs1048609704 |
| openSNP | rs1048609704 |
| 23andMe | rs1048609704 |
| SNPshot | rs1048609704 |
| SNPdbe | rs1048609704 |
| MSV3d | rs1048609704 |
| GWAS Ctlg | rs1048609704 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1048609704(G;G) |
| Alt | rs1048609704(G;G) |
| Reference | Rs1048609704(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.130699450A>G |
| CLNSRC | |
| CLNACC | RCV000484022.1, |
