rs7354779
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7354779(C;C) |
| Make rs7354779(C;T) |
| Make rs7354779(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44250887 |
| Gene | DNMT3L, LOC105372833 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7354779 |
| dbSNP (classic) | rs7354779 |
| ClinGen | rs7354779 |
| ebi | rs7354779 |
| HLI | rs7354779 |
| Exac | rs7354779 |
| Gnomad | rs7354779 |
| Varsome | rs7354779 |
| LitVar | rs7354779 |
| Map | rs7354779 |
| PheGenI | rs7354779 |
| Biobank | rs7354779 |
| 1000 genomes | rs7354779 |
| hgdp | rs7354779 |
| ensembl | rs7354779 |
| geneview | rs7354779 |
| scholar | rs7354779 |
| rs7354779 | |
| pharmgkb | rs7354779 |
| gwascentral | rs7354779 |
| openSNP | rs7354779 |
| 23andMe | rs7354779 |
| SNPshot | rs7354779 |
| SNPdbe | rs7354779 |
| MSV3d | rs7354779 |
| GWAS Ctlg | rs7354779 |
| GMAF | 0.1804 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 20593030
] Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking
[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 23922667] DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome
[PMID 26647998] Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility.
