rs1943950
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1943950(C;C) |
| Make rs1943950(C;T) |
| Make rs1943950(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 30107534 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1943950 |
| dbSNP (classic) | rs1943950 |
| ClinGen | rs1943950 |
| ebi | rs1943950 |
| HLI | rs1943950 |
| Exac | rs1943950 |
| Gnomad | rs1943950 |
| Varsome | rs1943950 |
| LitVar | rs1943950 |
| Map | rs1943950 |
| PheGenI | rs1943950 |
| Biobank | rs1943950 |
| 1000 genomes | rs1943950 |
| hgdp | rs1943950 |
| ensembl | rs1943950 |
| geneview | rs1943950 |
| scholar | rs1943950 |
| rs1943950 | |
| pharmgkb | rs1943950 |
| gwascentral | rs1943950 |
| openSNP | rs1943950 |
| 23andMe | rs1943950 |
| SNPshot | rs1943950 |
| SNPdbe | rs1943950 |
| MSV3d | rs1943950 |
| GWAS Ctlg | rs1943950 |
| GMAF | 0.1919 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23783273
] The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
