rs10770125
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10770125(A;A) |
| Make rs10770125(A;G) |
| Make rs10770125(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2147784 |
| Gene | IGF2, IGF2-AS, INS-IGF2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10770125 |
| dbSNP (classic) | rs10770125 |
| ClinGen | rs10770125 |
| ebi | rs10770125 |
| HLI | rs10770125 |
| Exac | rs10770125 |
| Gnomad | rs10770125 |
| Varsome | rs10770125 |
| LitVar | rs10770125 |
| Map | rs10770125 |
| PheGenI | rs10770125 |
| Biobank | rs10770125 |
| 1000 genomes | rs10770125 |
| hgdp | rs10770125 |
| ensembl | rs10770125 |
| geneview | rs10770125 |
| scholar | rs10770125 |
| rs10770125 | |
| pharmgkb | rs10770125 |
| gwascentral | rs10770125 |
| openSNP | rs10770125 |
| 23andMe | rs10770125 |
| SNPshot | rs10770125 |
| SNPdbe | rs10770125 |
| MSV3d | rs10770125 |
| GWAS Ctlg | rs10770125 |
| GMAF | 0.3848 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21926269
] Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy
[PMID 18769151] A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.
[PMID 28392167] Associations between a fetal imprinted gene allele score and late pregnancy maternal glucose concentrations.
