rs2847326
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2847326(A;A) |
| Make rs2847326(A;T) |
| Make rs2847326(T;T) |
| Reference | GRCh37.p10 37.5/138 |
| Chromosome | 18 |
| Position | 676228 |
| Gene | ENOSF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2847326 |
| dbSNP (classic) | rs2847326 |
| ClinGen | rs2847326 |
| ebi | rs2847326 |
| HLI | rs2847326 |
| Exac | rs2847326 |
| Gnomad | rs2847326 |
| Varsome | rs2847326 |
| LitVar | rs2847326 |
| Map | rs2847326 |
| PheGenI | rs2847326 |
| Biobank | rs2847326 |
| 1000 genomes | rs2847326 |
| hgdp | rs2847326 |
| ensembl | rs2847326 |
| geneview | rs2847326 |
| scholar | rs2847326 |
| rs2847326 | |
| pharmgkb | rs2847326 |
| gwascentral | rs2847326 |
| openSNP | rs2847326 |
| 23andMe | rs2847326 |
| SNPshot | rs2847326 |
| SNPdbe | rs2847326 |
| MSV3d | rs2847326 |
| GWAS Ctlg | rs2847326 |
| GMAF | 0.1745 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24535845
] Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways
