rs2612101
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2612101(C;C) |
| Make rs2612101(C;T) |
| Make rs2612101(T;T) |
| Reference | GRCh37.p10 37.5/138 |
| Chromosome | 18 |
| Position | 676473 |
| Gene | ENOSF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2612101 |
| dbSNP (classic) | rs2612101 |
| ClinGen | rs2612101 |
| ebi | rs2612101 |
| HLI | rs2612101 |
| Exac | rs2612101 |
| Gnomad | rs2612101 |
| Varsome | rs2612101 |
| LitVar | rs2612101 |
| Map | rs2612101 |
| PheGenI | rs2612101 |
| Biobank | rs2612101 |
| 1000 genomes | rs2612101 |
| hgdp | rs2612101 |
| ensembl | rs2612101 |
| geneview | rs2612101 |
| scholar | rs2612101 |
| rs2612101 | |
| pharmgkb | rs2612101 |
| gwascentral | rs2612101 |
| openSNP | rs2612101 |
| 23andMe | rs2612101 |
| SNPshot | rs2612101 |
| SNPdbe | rs2612101 |
| MSV3d | rs2612101 |
| GWAS Ctlg | rs2612101 |
| GMAF | 0.197 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24535845
] Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways
