rs114149656
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs114149656(C;T) |
| Make rs114149656(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 16188935 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs114149656 |
| dbSNP (classic) | rs114149656 |
| ClinGen | rs114149656 |
| ebi | rs114149656 |
| HLI | rs114149656 |
| Exac | rs114149656 |
| Gnomad | rs114149656 |
| Varsome | rs114149656 |
| LitVar | rs114149656 |
| Map | rs114149656 |
| PheGenI | rs114149656 |
| Biobank | rs114149656 |
| 1000 genomes | rs114149656 |
| hgdp | rs114149656 |
| ensembl | rs114149656 |
| geneview | rs114149656 |
| scholar | rs114149656 |
| rs114149656 | |
| pharmgkb | rs114149656 |
| gwascentral | rs114149656 |
| openSNP | rs114149656 |
| 23andMe | rs114149656 |
| SNPshot | rs114149656 |
| SNPdbe | rs114149656 |
| MSV3d | rs114149656 |
| GWAS Ctlg | rs114149656 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs114149656(A;A) rs114149656(T;T) |
| Alt | rs114149656(A;A) rs114149656(T;T) |
| Reference | Rs114149656(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.16282792C>A |
| CLNSRC | |
| CLNACC | RCV000424143.1, |
