rs1035139364
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1035139364(C;C) |
| Make rs1035139364(C;T) |
| Make rs1035139364(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 53308724 |
| Gene | AAAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1035139364 |
| dbSNP (classic) | rs1035139364 |
| ClinGen | rs1035139364 |
| ebi | rs1035139364 |
| HLI | rs1035139364 |
| Exac | rs1035139364 |
| Gnomad | rs1035139364 |
| Varsome | rs1035139364 |
| LitVar | rs1035139364 |
| Map | rs1035139364 |
| PheGenI | rs1035139364 |
| Biobank | rs1035139364 |
| 1000 genomes | rs1035139364 |
| hgdp | rs1035139364 |
| ensembl | rs1035139364 |
| geneview | rs1035139364 |
| scholar | rs1035139364 |
| rs1035139364 | |
| pharmgkb | rs1035139364 |
| gwascentral | rs1035139364 |
| openSNP | rs1035139364 |
| 23andMe | rs1035139364 |
| SNPshot | rs1035139364 |
| SNPdbe | rs1035139364 |
| MSV3d | rs1035139364 |
| GWAS Ctlg | rs1035139364 |
| Max Magnitude | 0 |
OMIM pathogenic
