rs12109442
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12109442(A;A) |
| Make rs12109442(A;T) |
| Make rs12109442(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 95827931 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12109442 |
| dbSNP (classic) | rs12109442 |
| ClinGen | rs12109442 |
| ebi | rs12109442 |
| HLI | rs12109442 |
| Exac | rs12109442 |
| Gnomad | rs12109442 |
| Varsome | rs12109442 |
| LitVar | rs12109442 |
| Map | rs12109442 |
| PheGenI | rs12109442 |
| Biobank | rs12109442 |
| 1000 genomes | rs12109442 |
| hgdp | rs12109442 |
| ensembl | rs12109442 |
| geneview | rs12109442 |
| scholar | rs12109442 |
| rs12109442 | |
| pharmgkb | rs12109442 |
| gwascentral | rs12109442 |
| openSNP | rs12109442 |
| 23andMe | rs12109442 |
| SNPshot | rs12109442 |
| SNPdbe | rs12109442 |
| MSV3d | rs12109442 |
| GWAS Ctlg | rs12109442 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 29399948
] A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.
