rs1062708
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1062708(C;C) |
| Make rs1062708(C;T) |
| Make rs1062708(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 49010016 |
| Gene | MIR6798, RUVBL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1062708 |
| dbSNP (classic) | rs1062708 |
| ClinGen | rs1062708 |
| ebi | rs1062708 |
| HLI | rs1062708 |
| Exac | rs1062708 |
| Gnomad | rs1062708 |
| Varsome | rs1062708 |
| LitVar | rs1062708 |
| Map | rs1062708 |
| PheGenI | rs1062708 |
| Biobank | rs1062708 |
| 1000 genomes | rs1062708 |
| hgdp | rs1062708 |
| ensembl | rs1062708 |
| geneview | rs1062708 |
| scholar | rs1062708 |
| rs1062708 | |
| pharmgkb | rs1062708 |
| gwascentral | rs1062708 |
| openSNP | rs1062708 |
| 23andMe | rs1062708 |
| SNPshot | rs1062708 |
| SNPdbe | rs1062708 |
| MSV3d | rs1062708 |
| GWAS Ctlg | rs1062708 |
| GMAF | 0.427 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
[PMID 16251468
] Survey of allelic expression using EST mining.
[PMID 19052777] Identification of common genetic variants that account for transcript isoform variation between human populations.
[PMID 19374514] Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.
