rs3830031
From SNPedia
| Merged into | rs1263791 |
| Orientation | plus |
| Stabilized | plus |
| Make rs3830031(A;A) |
| Make rs3830031(A;T) |
| Make rs3830031(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 21501530 |
| Gene | METTL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3830031 |
| dbSNP (classic) | rs3830031 |
| ClinGen | rs3830031 |
| ebi | rs3830031 |
| HLI | rs3830031 |
| Exac | rs3830031 |
| Gnomad | rs3830031 |
| Varsome | rs3830031 |
| LitVar | rs3830031 |
| Map | rs3830031 |
| PheGenI | rs3830031 |
| Biobank | rs3830031 |
| 1000 genomes | rs3830031 |
| hgdp | rs3830031 |
| ensembl | rs3830031 |
| geneview | rs3830031 |
| scholar | rs3830031 |
| rs3830031 | |
| pharmgkb | rs3830031 |
| gwascentral | rs3830031 |
| openSNP | rs3830031 |
| 23andMe | rs3830031 |
| SNPshot | rs3830031 |
| SNPdbe | rs3830031 |
| MSV3d | rs3830031 |
| GWAS Ctlg | rs3830031 |
| Status | Merged into rs1263791 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20523082] Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population
