rs10007186
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10007186(C;C) |
| Make rs10007186(C;T) |
| Make rs10007186(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 78667891 |
| Gene | LINC01094 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10007186 |
| dbSNP (classic) | rs10007186 |
| ClinGen | rs10007186 |
| ebi | rs10007186 |
| HLI | rs10007186 |
| Exac | rs10007186 |
| Gnomad | rs10007186 |
| Varsome | rs10007186 |
| LitVar | rs10007186 |
| Map | rs10007186 |
| PheGenI | rs10007186 |
| Biobank | rs10007186 |
| 1000 genomes | rs10007186 |
| hgdp | rs10007186 |
| ensembl | rs10007186 |
| geneview | rs10007186 |
| scholar | rs10007186 |
| rs10007186 | |
| pharmgkb | rs10007186 |
| gwascentral | rs10007186 |
| openSNP | rs10007186 |
| 23andMe | rs10007186 |
| SNPshot | rs10007186 |
| SNPdbe | rs10007186 |
| MSV3d | rs10007186 |
| GWAS Ctlg | rs10007186 |
| GMAF | 0.3664 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22558069 ]
|
| Trait | |
| Title | Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. |
| Risk Allele | C |
| P-val | 1E-9 |
| Odds Ratio | 0.0850 None |
