rs16999358
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs16999358(A;A) |
| Make rs16999358(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 19 |
| Position | 10162679 |
| Gene | DNMT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16999358 |
| dbSNP (classic) | rs16999358 |
| ClinGen | rs16999358 |
| ebi | rs16999358 |
| HLI | rs16999358 |
| Exac | rs16999358 |
| Gnomad | rs16999358 |
| Varsome | rs16999358 |
| LitVar | rs16999358 |
| Map | rs16999358 |
| PheGenI | rs16999358 |
| Biobank | rs16999358 |
| 1000 genomes | rs16999358 |
| hgdp | rs16999358 |
| ensembl | rs16999358 |
| geneview | rs16999358 |
| scholar | rs16999358 |
| rs16999358 | |
| pharmgkb | rs16999358 |
| gwascentral | rs16999358 |
| openSNP | rs16999358 |
| 23andMe | rs16999358 |
| SNPshot | rs16999358 |
| SNPdbe | rs16999358 |
| MSV3d | rs16999358 |
| GWAS Ctlg | rs16999358 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28323001] DNA methyltransferase 1 rs16999593 genetic polymorphism decreases risk in patients with transposition of great arteries.
| ClinVar | |
|---|---|
| Risk | rs16999358(A;A) |
| Alt | rs16999358(A;A) |
| Reference | Rs16999358(G;G) |
| Significance | Non-pathogenic |
| Disease | Dementia |
| Variation | info |
| Gene | DNMT1 |
| CLNDBN | Dementia, Deafness, and Sensory Neuropathy |
| Reversed | 0 |
| HGVS | NC_000019.9:g.10273355G>A |
| CLNSRC | |
| CLNACC | RCV000379095.1, |
