rs77542162
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (A;A) | 0 | common genotype | 
| Make rs77542162(A;G) | 
| Make rs77542162(G;G) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 17 | 
| Position | 69085137 | 
| Gene | ABCA6 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs77542162 | 
| dbSNP (classic) | rs77542162 | 
| ClinGen | rs77542162 | 
| ebi | rs77542162 | 
| HLI | rs77542162 | 
| Exac | rs77542162 | 
| Gnomad | rs77542162 | 
| Varsome | rs77542162 | 
| LitVar | rs77542162 | 
| Map | rs77542162 | 
| PheGenI | rs77542162 | 
| Biobank | rs77542162 | 
| 1000 genomes | rs77542162 | 
| hgdp | rs77542162 | 
| ensembl | rs77542162 | 
| geneview | rs77542162 | 
| scholar | rs77542162 | 
| rs77542162 | |
| pharmgkb | rs77542162 | 
| gwascentral | rs77542162 | 
| openSNP | rs77542162 | 
| 23andMe | rs77542162 | 
| SNPshot | rs77542162 | 
| SNPdbe | rs77542162 | 
| MSV3d | rs77542162 | 
| GWAS Ctlg | rs77542162 | 
| 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.


