rs1021156
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1021156(A;A) |
| Make rs1021156(A;G) |
| Make rs1021156(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 8 |
| Position | 78663569 |
| Gene | LOC105375911 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1021156 |
| dbSNP (classic) | rs1021156 |
| ClinGen | rs1021156 |
| ebi | rs1021156 |
| HLI | rs1021156 |
| Exac | rs1021156 |
| Gnomad | rs1021156 |
| Varsome | rs1021156 |
| LitVar | rs1021156 |
| Map | rs1021156 |
| PheGenI | rs1021156 |
| Biobank | rs1021156 |
| 1000 genomes | rs1021156 |
| hgdp | rs1021156 |
| ensembl | rs1021156 |
| geneview | rs1021156 |
| scholar | rs1021156 |
| rs1021156 | |
| pharmgkb | rs1021156 |
| gwascentral | rs1021156 |
| openSNP | rs1021156 |
| 23andMe | rs1021156 |
| SNPshot | rs1021156 |
| SNPdbe | rs1021156 |
| MSV3d | rs1021156 |
| GWAS Ctlg | rs1021156 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 27559181] Role of genetic susceptibility variants in predicting clinical course in multiple sclerosis: a cohort study.
