rs1893379
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1893379(C;C) |
| Make rs1893379(C;T) |
| Make rs1893379(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 51192166 |
| Gene | MEX3C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1893379 |
| dbSNP (classic) | rs1893379 |
| ClinGen | rs1893379 |
| ebi | rs1893379 |
| HLI | rs1893379 |
| Exac | rs1893379 |
| Gnomad | rs1893379 |
| Varsome | rs1893379 |
| LitVar | rs1893379 |
| Map | rs1893379 |
| PheGenI | rs1893379 |
| Biobank | rs1893379 |
| 1000 genomes | rs1893379 |
| hgdp | rs1893379 |
| ensembl | rs1893379 |
| geneview | rs1893379 |
| scholar | rs1893379 |
| rs1893379 | |
| pharmgkb | rs1893379 |
| gwascentral | rs1893379 |
| openSNP | rs1893379 |
| 23andMe | rs1893379 |
| SNPshot | rs1893379 |
| SNPdbe | rs1893379 |
| MSV3d | rs1893379 |
| GWAS Ctlg | rs1893379 |
| GMAF | 0.309 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 15532013
] Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy.
[PMID 17015768] Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.
