rs56489998
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs56489998(C;C) |
| Make rs56489998(C;T) |
| Make rs56489998(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | MT |
| Position | 663 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56489998 |
| dbSNP (classic) | rs56489998 |
| ClinGen | rs56489998 |
| ebi | rs56489998 |
| HLI | rs56489998 |
| Exac | rs56489998 |
| Gnomad | rs56489998 |
| Varsome | rs56489998 |
| LitVar | rs56489998 |
| Map | rs56489998 |
| PheGenI | rs56489998 |
| Biobank | rs56489998 |
| 1000 genomes | rs56489998 |
| hgdp | rs56489998 |
| ensembl | rs56489998 |
| geneview | rs56489998 |
| scholar | rs56489998 |
| rs56489998 | |
| pharmgkb | rs56489998 |
| gwascentral | rs56489998 |
| openSNP | rs56489998 |
| 23andMe | rs56489998 |
| SNPshot | rs56489998 |
| SNPdbe | rs56489998 |
| MSV3d | rs56489998 |
| GWAS Ctlg | rs56489998 |
| Merged from | Rs3937039 |
| GMAF | 0.07951 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19458495
] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
