rs781065280
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs781065280(A;A) |
| Make rs781065280(A;G) |
| Make rs781065280(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 14 |
| Position | 64419926 |
| Gene | MTHFD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs781065280 |
| dbSNP (classic) | rs781065280 |
| ClinGen | rs781065280 |
| ebi | rs781065280 |
| HLI | rs781065280 |
| Exac | rs781065280 |
| Gnomad | rs781065280 |
| Varsome | rs781065280 |
| LitVar | rs781065280 |
| Map | rs781065280 |
| PheGenI | rs781065280 |
| Biobank | rs781065280 |
| 1000 genomes | rs781065280 |
| hgdp | rs781065280 |
| ensembl | rs781065280 |
| geneview | rs781065280 |
| scholar | rs781065280 |
| rs781065280 | |
| pharmgkb | rs781065280 |
| gwascentral | rs781065280 |
| openSNP | rs781065280 |
| 23andMe | rs781065280 |
| SNPshot | rs781065280 |
| SNPdbe | rs781065280 |
| MSV3d | rs781065280 |
| GWAS Ctlg | rs781065280 |
| Max Magnitude | 0 |
aka NM_005956.3(MTHFD1):c.727+1G>A
OMIM pathogenic variant
