rs371848318
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs371848318(A;A) |
| Make rs371848318(A;G) |
| Make rs371848318(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 1 |
| Position | 45341543 |
| Gene | MUTYH, TOE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371848318 |
| dbSNP (classic) | rs371848318 |
| ClinGen | rs371848318 |
| ebi | rs371848318 |
| HLI | rs371848318 |
| Exac | rs371848318 |
| Gnomad | rs371848318 |
| Varsome | rs371848318 |
| LitVar | rs371848318 |
| Map | rs371848318 |
| PheGenI | rs371848318 |
| Biobank | rs371848318 |
| 1000 genomes | rs371848318 |
| hgdp | rs371848318 |
| ensembl | rs371848318 |
| geneview | rs371848318 |
| scholar | rs371848318 |
| rs371848318 | |
| pharmgkb | rs371848318 |
| gwascentral | rs371848318 |
| openSNP | rs371848318 |
| 23andMe | rs371848318 |
| SNPshot | rs371848318 |
| SNPdbe | rs371848318 |
| MSV3d | rs371848318 |
| GWAS Ctlg | rs371848318 |
| Max Magnitude | 0 |
aka NM_025077.3(TOE1):c.307G>A or (p.Ala103Thr)
OMIM pathogenic variant
