rs2067051
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2067051(A;A) |
| Make rs2067051(A;G) |
| Make rs2067051(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 1996938 |
| Gene | H19, MIR675, MRPL23 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2067051 |
| dbSNP (classic) | rs2067051 |
| ClinGen | rs2067051 |
| ebi | rs2067051 |
| HLI | rs2067051 |
| Exac | rs2067051 |
| Gnomad | rs2067051 |
| Varsome | rs2067051 |
| LitVar | rs2067051 |
| Map | rs2067051 |
| PheGenI | rs2067051 |
| Biobank | rs2067051 |
| 1000 genomes | rs2067051 |
| hgdp | rs2067051 |
| ensembl | rs2067051 |
| geneview | rs2067051 |
| scholar | rs2067051 |
| rs2067051 | |
| pharmgkb | rs2067051 |
| gwascentral | rs2067051 |
| openSNP | rs2067051 |
| 23andMe | rs2067051 |
| SNPshot | rs2067051 |
| SNPdbe | rs2067051 |
| MSV3d | rs2067051 |
| GWAS Ctlg | rs2067051 |
| GMAF | 0.3448 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20639793
] Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes
[PMID 15885138] Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.
[PMID 16839189] Human imprinted chromosomal regions are historical hot-spots of recombination.
