rs270102
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs270102(A;G) |
| Make rs270102(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 25109771 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs270102 |
| dbSNP (classic) | rs270102 |
| ClinGen | rs270102 |
| ebi | rs270102 |
| HLI | rs270102 |
| Exac | rs270102 |
| Gnomad | rs270102 |
| Varsome | rs270102 |
| LitVar | rs270102 |
| Map | rs270102 |
| PheGenI | rs270102 |
| Biobank | rs270102 |
| 1000 genomes | rs270102 |
| hgdp | rs270102 |
| ensembl | rs270102 |
| geneview | rs270102 |
| scholar | rs270102 |
| rs270102 | |
| pharmgkb | rs270102 |
| gwascentral | rs270102 |
| openSNP | rs270102 |
| 23andMe | rs270102 |
| SNPshot | rs270102 |
| SNPdbe | rs270102 |
| MSV3d | rs270102 |
| GWAS Ctlg | rs270102 |
| Max Magnitude | 0 |
[PMID 19456320
] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
