rs141923065
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs141923065(A;A) |
| Make rs141923065(A;G) |
| Make rs141923065(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 31462770 |
| Gene | ARMC5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141923065 |
| dbSNP (classic) | rs141923065 |
| ClinGen | rs141923065 |
| ebi | rs141923065 |
| HLI | rs141923065 |
| Exac | rs141923065 |
| Gnomad | rs141923065 |
| Varsome | rs141923065 |
| LitVar | rs141923065 |
| Map | rs141923065 |
| PheGenI | rs141923065 |
| Biobank | rs141923065 |
| 1000 genomes | rs141923065 |
| hgdp | rs141923065 |
| ensembl | rs141923065 |
| geneview | rs141923065 |
| scholar | rs141923065 |
| rs141923065 | |
| pharmgkb | rs141923065 |
| gwascentral | rs141923065 |
| openSNP | rs141923065 |
| 23andMe | rs141923065 |
| SNPshot | rs141923065 |
| SNPdbe | rs141923065 |
| MSV3d | rs141923065 |
| GWAS Ctlg | rs141923065 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
