rs370444838
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs370444838(C;C) |
| Make rs370444838(C;T) |
| Make rs370444838(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 14 |
| Position | 64411109 |
| Gene | MTHFD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs370444838 |
| dbSNP (classic) | rs370444838 |
| ClinGen | rs370444838 |
| ebi | rs370444838 |
| HLI | rs370444838 |
| Exac | rs370444838 |
| Gnomad | rs370444838 |
| Varsome | rs370444838 |
| LitVar | rs370444838 |
| Map | rs370444838 |
| PheGenI | rs370444838 |
| Biobank | rs370444838 |
| 1000 genomes | rs370444838 |
| hgdp | rs370444838 |
| ensembl | rs370444838 |
| geneview | rs370444838 |
| scholar | rs370444838 |
| rs370444838 | |
| pharmgkb | rs370444838 |
| gwascentral | rs370444838 |
| openSNP | rs370444838 |
| 23andMe | rs370444838 |
| SNPshot | rs370444838 |
| SNPdbe | rs370444838 |
| MSV3d | rs370444838 |
| GWAS Ctlg | rs370444838 |
| Max Magnitude | 0 |
aka NM_005956.3(MTHFD1):c.146C>T or (p.Ser49Phe)
OMIM pathogenic variant
