rs104894193
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs104894193(A;A) |
| Make rs104894193(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 44275472 |
| Gene | ALX4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104894193 |
| dbSNP (classic) | rs104894193 |
| ClinGen | rs104894193 |
| ebi | rs104894193 |
| HLI | rs104894193 |
| Exac | rs104894193 |
| Gnomad | rs104894193 |
| Varsome | rs104894193 |
| LitVar | rs104894193 |
| Map | rs104894193 |
| PheGenI | rs104894193 |
| Biobank | rs104894193 |
| 1000 genomes | rs104894193 |
| hgdp | rs104894193 |
| ensembl | rs104894193 |
| geneview | rs104894193 |
| scholar | rs104894193 |
| rs104894193 | |
| pharmgkb | rs104894193 |
| gwascentral | rs104894193 |
| openSNP | rs104894193 |
| 23andMe | rs104894193 |
| SNPshot | rs104894193 |
| SNPdbe | rs104894193 |
| MSV3d | rs104894193 |
| GWAS Ctlg | rs104894193 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs104894193(A;A) |
| Alt | rs104894193(A;A) |
| Reference | Rs104894193(G;G) |
| Significance | Pathogenic |
| Disease | Parietal foramina 2 |
| Variation | info |
| Gene | ALX4 |
| CLNDBN | Parietal foramina 2 |
| Reversed | 1 |
| HGVS | NC_000011.9:g.44297022C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000005318.5, |
[PMID 16319823
] Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
