rs2671641
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2671641(C;C) |
| Make rs2671641(C;G) |
| Make rs2671641(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 17 |
| Position | 49520365 |
| Gene | LOC100288866 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2671641 |
| dbSNP (classic) | rs2671641 |
| ClinGen | rs2671641 |
| ebi | rs2671641 |
| HLI | rs2671641 |
| Exac | rs2671641 |
| Gnomad | rs2671641 |
| Varsome | rs2671641 |
| LitVar | rs2671641 |
| Map | rs2671641 |
| PheGenI | rs2671641 |
| Biobank | rs2671641 |
| 1000 genomes | rs2671641 |
| hgdp | rs2671641 |
| ensembl | rs2671641 |
| geneview | rs2671641 |
| scholar | rs2671641 |
| rs2671641 | |
| pharmgkb | rs2671641 |
| gwascentral | rs2671641 |
| openSNP | rs2671641 |
| 23andMe | rs2671641 |
| SNPshot | rs2671641 |
| SNPdbe | rs2671641 |
| MSV3d | rs2671641 |
| GWAS Ctlg | rs2671641 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25227100] Selection of human p75NTR tag SNPs and its biological significance for clinical association studies
