rs4929984
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4929984(A;A) |
| Make rs4929984(A;C) |
| Make rs4929984(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2003453 |
| Gene | H19, MRPL23 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4929984 |
| dbSNP (classic) | rs4929984 |
| ClinGen | rs4929984 |
| ebi | rs4929984 |
| HLI | rs4929984 |
| Exac | rs4929984 |
| Gnomad | rs4929984 |
| Varsome | rs4929984 |
| LitVar | rs4929984 |
| Map | rs4929984 |
| PheGenI | rs4929984 |
| Biobank | rs4929984 |
| 1000 genomes | rs4929984 |
| hgdp | rs4929984 |
| ensembl | rs4929984 |
| geneview | rs4929984 |
| scholar | rs4929984 |
| rs4929984 | |
| pharmgkb | rs4929984 |
| gwascentral | rs4929984 |
| openSNP | rs4929984 |
| 23andMe | rs4929984 |
| SNPshot | rs4929984 |
| SNPdbe | rs4929984 |
| MSV3d | rs4929984 |
| GWAS Ctlg | rs4929984 |
| GMAF | 0.4123 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20639793
] Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes
[PMID 16839189] Human imprinted chromosomal regions are historical hot-spots of recombination.
