rs761413864
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs761413864(A;G) |
| Make rs761413864(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 113282867 |
| Gene | ANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761413864 |
| dbSNP (classic) | rs761413864 |
| ClinGen | rs761413864 |
| ebi | rs761413864 |
| HLI | rs761413864 |
| Exac | rs761413864 |
| Gnomad | rs761413864 |
| Varsome | rs761413864 |
| LitVar | rs761413864 |
| Map | rs761413864 |
| PheGenI | rs761413864 |
| Biobank | rs761413864 |
| 1000 genomes | rs761413864 |
| hgdp | rs761413864 |
| ensembl | rs761413864 |
| geneview | rs761413864 |
| scholar | rs761413864 |
| rs761413864 | |
| pharmgkb | rs761413864 |
| gwascentral | rs761413864 |
| openSNP | rs761413864 |
| 23andMe | rs761413864 |
| SNPshot | rs761413864 |
| SNPdbe | rs761413864 |
| MSV3d | rs761413864 |
| GWAS Ctlg | rs761413864 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs761413864(G;G) |
| Alt | rs761413864(G;G) |
| Reference | Rs761413864(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ANK2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.114204023A>G |
| CLNSRC | |
| CLNACC | RCV000170729.3, |
