rs2276248
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2276248(C;C) |
| Make rs2276248(C;T) |
| Make rs2276248(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44259375 |
| Gene | DNMT3L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2276248 |
| dbSNP (classic) | rs2276248 |
| ClinGen | rs2276248 |
| ebi | rs2276248 |
| HLI | rs2276248 |
| Exac | rs2276248 |
| Gnomad | rs2276248 |
| Varsome | rs2276248 |
| LitVar | rs2276248 |
| Map | rs2276248 |
| PheGenI | rs2276248 |
| Biobank | rs2276248 |
| 1000 genomes | rs2276248 |
| hgdp | rs2276248 |
| ensembl | rs2276248 |
| geneview | rs2276248 |
| scholar | rs2276248 |
| rs2276248 | |
| pharmgkb | rs2276248 |
| gwascentral | rs2276248 |
| openSNP | rs2276248 |
| 23andMe | rs2276248 |
| SNPshot | rs2276248 |
| SNPdbe | rs2276248 |
| MSV3d | rs2276248 |
| GWAS Ctlg | rs2276248 |
| GMAF | 0.1281 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22116073] Association between single-nucleotide polymorphisms of DNMT3L and infertility with azoospermia in Chinese men
[PMID 22401780] Genetic polymorphisms of DNMT3L involved in hypermethylation of chromosomal ends are associated with greater risk of developing ovarian endometriosis.
[PMID 26647998] Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility.
