rs1313770
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1313770(A;A) |
| Make rs1313770(A;G) |
| Make rs1313770(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 3056082 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1313770 |
| dbSNP (classic) | rs1313770 |
| ClinGen | rs1313770 |
| ebi | rs1313770 |
| HLI | rs1313770 |
| Exac | rs1313770 |
| Gnomad | rs1313770 |
| Varsome | rs1313770 |
| LitVar | rs1313770 |
| Map | rs1313770 |
| PheGenI | rs1313770 |
| Biobank | rs1313770 |
| 1000 genomes | rs1313770 |
| hgdp | rs1313770 |
| ensembl | rs1313770 |
| geneview | rs1313770 |
| scholar | rs1313770 |
| rs1313770 | |
| pharmgkb | rs1313770 |
| gwascentral | rs1313770 |
| openSNP | rs1313770 |
| 23andMe | rs1313770 |
| SNPshot | rs1313770 |
| SNPdbe | rs1313770 |
| MSV3d | rs1313770 |
| GWAS Ctlg | rs1313770 |
| GMAF | 0.4614 |
| Max Magnitude | 0 |
[PMID 15832309] Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
