rs760889414
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs760889414(G;G) |
| Make rs760889414(G;T) |
| Make rs760889414(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 14 |
| Position | 64419871 |
| Gene | MTHFD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760889414 |
| dbSNP (classic) | rs760889414 |
| ClinGen | rs760889414 |
| ebi | rs760889414 |
| HLI | rs760889414 |
| Exac | rs760889414 |
| Gnomad | rs760889414 |
| Varsome | rs760889414 |
| LitVar | rs760889414 |
| Map | rs760889414 |
| PheGenI | rs760889414 |
| Biobank | rs760889414 |
| 1000 genomes | rs760889414 |
| hgdp | rs760889414 |
| ensembl | rs760889414 |
| geneview | rs760889414 |
| scholar | rs760889414 |
| rs760889414 | |
| pharmgkb | rs760889414 |
| gwascentral | rs760889414 |
| openSNP | rs760889414 |
| 23andMe | rs760889414 |
| SNPshot | rs760889414 |
| SNPdbe | rs760889414 |
| MSV3d | rs760889414 |
| GWAS Ctlg | rs760889414 |
| Max Magnitude | 0 |
aka NM_005956.3(MTHFD1):c.673G>T or (p.Glu225Ter)
OMIM pathogenic variant
