rs749346955
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs749346955(A;A) |
| Make rs749346955(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 15 |
| Position | 37093609 |
| Gene | MEIS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs749346955 |
| dbSNP (classic) | rs749346955 |
| ClinGen | rs749346955 |
| ebi | rs749346955 |
| HLI | rs749346955 |
| Exac | rs749346955 |
| Gnomad | rs749346955 |
| Varsome | rs749346955 |
| LitVar | rs749346955 |
| Map | rs749346955 |
| PheGenI | rs749346955 |
| Biobank | rs749346955 |
| 1000 genomes | rs749346955 |
| hgdp | rs749346955 |
| ensembl | rs749346955 |
| geneview | rs749346955 |
| scholar | rs749346955 |
| rs749346955 | |
| pharmgkb | rs749346955 |
| gwascentral | rs749346955 |
| openSNP | rs749346955 |
| 23andMe | rs749346955 |
| SNPshot | rs749346955 |
| SNPdbe | rs749346955 |
| MSV3d | rs749346955 |
| GWAS Ctlg | rs749346955 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs749346955(A;A) rs749346955(C;C) |
| Alt | rs749346955(A;A) rs749346955(C;C) |
| Reference | Rs749346955(G;G) |
| Significance | Pathogenic |
| Disease | Cleft palate |
| Variation | info |
| Gene | MEIS2 |
| CLNDBN | Cleft palate, cardiac defects, and mental retardation |
| Reversed | 0 |
| HGVS | NC_000015.9:g.37385810G>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000490249.2, |
