rs151181674
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs151181674(C;C) |
| Make rs151181674(C;T) |
| Make rs151181674(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 16986334 |
| Gene | ATP13A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs151181674 |
| dbSNP (classic) | rs151181674 |
| ClinGen | rs151181674 |
| ebi | rs151181674 |
| HLI | rs151181674 |
| Exac | rs151181674 |
| Gnomad | rs151181674 |
| Varsome | rs151181674 |
| LitVar | rs151181674 |
| Map | rs151181674 |
| PheGenI | rs151181674 |
| Biobank | rs151181674 |
| 1000 genomes | rs151181674 |
| hgdp | rs151181674 |
| ensembl | rs151181674 |
| geneview | rs151181674 |
| scholar | rs151181674 |
| rs151181674 | |
| pharmgkb | rs151181674 |
| gwascentral | rs151181674 |
| openSNP | rs151181674 |
| 23andMe | rs151181674 |
| SNPshot | rs151181674 |
| SNPdbe | rs151181674 |
| MSV3d | rs151181674 |
| GWAS Ctlg | rs151181674 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs151181674(T;T) |
| Alt | rs151181674(T;T) |
| Reference | rs151181674(C;C) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | ATP13A2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000001.10:g.17312829C>T |
| CLNSRC | |
| CLNACC | RCV000116443.3, |
