rs11861980
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs11861980(A;A) |
| Make rs11861980(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16173376 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11861980 |
| dbSNP (classic) | rs11861980 |
| ClinGen | rs11861980 |
| ebi | rs11861980 |
| HLI | rs11861980 |
| Exac | rs11861980 |
| Gnomad | rs11861980 |
| Varsome | rs11861980 |
| LitVar | rs11861980 |
| Map | rs11861980 |
| PheGenI | rs11861980 |
| Biobank | rs11861980 |
| 1000 genomes | rs11861980 |
| hgdp | rs11861980 |
| ensembl | rs11861980 |
| geneview | rs11861980 |
| scholar | rs11861980 |
| rs11861980 | |
| pharmgkb | rs11861980 |
| gwascentral | rs11861980 |
| openSNP | rs11861980 |
| 23andMe | rs11861980 |
| SNPshot | rs11861980 |
| SNPdbe | rs11861980 |
| MSV3d | rs11861980 |
| GWAS Ctlg | rs11861980 |
| GMAF | 0.003214 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs11861980(A;A) rs11861980(C;C) |
| Alt | rs11861980(A;A) rs11861980(C;C) |
| Reference | Rs11861980(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.16267233G>C |
| CLNSRC | |
| CLNACC | |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
