rs2847607
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2847607(A;A) |
| Make rs2847607(A;G) |
| Make rs2847607(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 18 |
| Position | 681724 |
| Gene | ENOSF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2847607 |
| dbSNP (classic) | rs2847607 |
| ClinGen | rs2847607 |
| ebi | rs2847607 |
| HLI | rs2847607 |
| Exac | rs2847607 |
| Gnomad | rs2847607 |
| Varsome | rs2847607 |
| LitVar | rs2847607 |
| Map | rs2847607 |
| PheGenI | rs2847607 |
| Biobank | rs2847607 |
| 1000 genomes | rs2847607 |
| hgdp | rs2847607 |
| ensembl | rs2847607 |
| geneview | rs2847607 |
| scholar | rs2847607 |
| rs2847607 | |
| pharmgkb | rs2847607 |
| gwascentral | rs2847607 |
| openSNP | rs2847607 |
| 23andMe | rs2847607 |
| SNPshot | rs2847607 |
| SNPdbe | rs2847607 |
| MSV3d | rs2847607 |
| GWAS Ctlg | rs2847607 |
| GMAF | 0.163 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24535845
] Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways
