rs72338773
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in complete genomics |
| Make rs72338773(-;GGGCGCTGT) |
| Make rs72338773(GGGCGCTGT;GGGCGCTGT) |
| Reference | GRCh37.p10 37.5/138 |
| Chromosome | 17 |
| Position | 46608203 |
| Gene | HOXB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72338773 |
| dbSNP (classic) | rs72338773 |
| ClinGen | rs72338773 |
| ebi | rs72338773 |
| HLI | rs72338773 |
| Exac | rs72338773 |
| Gnomad | rs72338773 |
| Varsome | rs72338773 |
| LitVar | rs72338773 |
| Map | rs72338773 |
| PheGenI | rs72338773 |
| Biobank | rs72338773 |
| 1000 genomes | rs72338773 |
| hgdp | rs72338773 |
| ensembl | rs72338773 |
| geneview | rs72338773 |
| scholar | rs72338773 |
| rs72338773 | |
| pharmgkb | rs72338773 |
| gwascentral | rs72338773 |
| openSNP | rs72338773 |
| 23andMe | rs72338773 |
| SNPshot | rs72338773 |
| SNPdbe | rs72338773 |
| MSV3d | rs72338773 |
| GWAS Ctlg | rs72338773 |
| Status | Deleted |
| Max Magnitude | 0 |
[PMID 20678259
] Candidate gene study of HOXB1 in autism spectrum disorder
[PMID 21980499] An Integrated Meta-Analysis of Two Variants in HOXA1/HOXB1 and Their Effect on the Risk of Autism Spectrum Disorders
