rs41286560
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs41286560(G;G) | 
| Make rs41286560(G;T) | 
| Make rs41286560(T;T) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 14 | 
| Position | 100883117 | 
| Gene | MIR127, MIR136, MIR432, RTL1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs41286560 | 
| dbSNP (classic) | rs41286560 | 
| ClinGen | rs41286560 | 
| ebi | rs41286560 | 
| HLI | rs41286560 | 
| Exac | rs41286560 | 
| Gnomad | rs41286560 | 
| Varsome | rs41286560 | 
| LitVar | rs41286560 | 
| Map | rs41286560 | 
| PheGenI | rs41286560 | 
| Biobank | rs41286560 | 
| 1000 genomes | rs41286560 | 
| hgdp | rs41286560 | 
| ensembl | rs41286560 | 
| geneview | rs41286560 | 
| scholar | rs41286560 | 
| rs41286560 | |
| pharmgkb | rs41286560 | 
| gwascentral | rs41286560 | 
| openSNP | rs41286560 | 
| 23andMe | rs41286560 | 
| SNPshot | rs41286560 | 
| SNPdbe | rs41286560 | 
| MSV3d | rs41286560 | 
| GWAS Ctlg | rs41286560 | 
| Max Magnitude | 0 | 
[PMID 28146470 ] Rare and low-frequency coding variants alter human adult height.
] Rare and low-frequency coding variants alter human adult height.


