rs373900644
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 3 | Carrier of an orofaciodigital mutation |
| (T;T) | 9 | Orofaciodigital syndrome likely |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 127663438 |
| Gene | INTU |
| is a | snp |
| is | mentioned by |
| dbSNP | rs373900644 |
| dbSNP (classic) | rs373900644 |
| ClinGen | rs373900644 |
| ebi | rs373900644 |
| HLI | rs373900644 |
| Exac | rs373900644 |
| Gnomad | rs373900644 |
| Varsome | rs373900644 |
| LitVar | rs373900644 |
| Map | rs373900644 |
| PheGenI | rs373900644 |
| Biobank | rs373900644 |
| 1000 genomes | rs373900644 |
| hgdp | rs373900644 |
| ensembl | rs373900644 |
| geneview | rs373900644 |
| scholar | rs373900644 |
| rs373900644 | |
| pharmgkb | rs373900644 |
| gwascentral | rs373900644 |
| openSNP | rs373900644 |
| 23andMe | rs373900644 |
| SNPshot | rs373900644 |
| SNPdbe | rs373900644 |
| MSV3d | rs373900644 |
| GWAS Ctlg | rs373900644 |
| Max Magnitude | 9 |
23andMe calls this i6023169
see [PMID 27158779
]
