rs3741205
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3741205(G;G) |
| Make rs3741205(G;T) |
| Make rs3741205(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2148654 |
| Gene | IGF2, IGF2-AS, INS-IGF2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3741205 |
| dbSNP (classic) | rs3741205 |
| ClinGen | rs3741205 |
| ebi | rs3741205 |
| HLI | rs3741205 |
| Exac | rs3741205 |
| Gnomad | rs3741205 |
| Varsome | rs3741205 |
| LitVar | rs3741205 |
| Map | rs3741205 |
| PheGenI | rs3741205 |
| Biobank | rs3741205 |
| 1000 genomes | rs3741205 |
| hgdp | rs3741205 |
| ensembl | rs3741205 |
| geneview | rs3741205 |
| scholar | rs3741205 |
| rs3741205 | |
| pharmgkb | rs3741205 |
| gwascentral | rs3741205 |
| openSNP | rs3741205 |
| 23andMe | rs3741205 |
| SNPshot | rs3741205 |
| SNPdbe | rs3741205 |
| MSV3d | rs3741205 |
| GWAS Ctlg | rs3741205 |
| GMAF | 0.3384 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20639793
] Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes
[PMID 28443481] Impact of Abnormal DNA Methylation of Imprinted Loci on Human Spontaneous Abortion.
