rs1046778
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1046778(C;C) |
| Make rs1046778(C;T) |
| Make rs1046778(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 102901727 |
| Gene | AS3MT, BORCS7-ASMT, LOC107984265 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1046778 |
| dbSNP (classic) | rs1046778 |
| ClinGen | rs1046778 |
| ebi | rs1046778 |
| HLI | rs1046778 |
| Exac | rs1046778 |
| Gnomad | rs1046778 |
| Varsome | rs1046778 |
| LitVar | rs1046778 |
| Map | rs1046778 |
| PheGenI | rs1046778 |
| Biobank | rs1046778 |
| 1000 genomes | rs1046778 |
| hgdp | rs1046778 |
| ensembl | rs1046778 |
| geneview | rs1046778 |
| scholar | rs1046778 |
| rs1046778 | |
| pharmgkb | rs1046778 |
| gwascentral | rs1046778 |
| openSNP | rs1046778 |
| 23andMe | rs1046778 |
| SNPshot | rs1046778 |
| SNPdbe | rs1046778 |
| MSV3d | rs1046778 |
| GWAS Ctlg | rs1046778 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 25156000
] Genetic variation in arsenic (+3 oxidation state) methyltransferase (AS3MT), arsenic metabolism and risk of basal cell carcinoma in a European population
[PMID 26928318] Analysis of maternal polymorphisms in arsenic (+3 oxidation state)-methyltransferase AS3MT and fetal sex in relation to arsenic metabolism and infant birth outcomes: implications for risk analysis.
