rs267606559
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (I;I) | 0 | common genotype |
| Make rs267606559(-;-) |
| Make rs267606559(-;T) |
| Make rs267606559(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 67490111 |
| Gene | AIP, MIR6752 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267606559 |
| dbSNP (classic) | rs267606559 |
| ClinGen | rs267606559 |
| ebi | rs267606559 |
| HLI | rs267606559 |
| Exac | rs267606559 |
| Gnomad | rs267606559 |
| Varsome | rs267606559 |
| LitVar | rs267606559 |
| Map | rs267606559 |
| PheGenI | rs267606559 |
| Biobank | rs267606559 |
| 1000 genomes | rs267606559 |
| hgdp | rs267606559 |
| ensembl | rs267606559 |
| geneview | rs267606559 |
| scholar | rs267606559 |
| rs267606559 | |
| pharmgkb | rs267606559 |
| gwascentral | rs267606559 |
| openSNP | rs267606559 |
| 23andMe | rs267606559 |
| SNPshot | rs267606559 |
| SNPdbe | rs267606559 |
| MSV3d | rs267606559 |
| GWAS Ctlg | rs267606559 |
| Max Magnitude | 0 |
OMIM pathogenic variant
