rs16942341
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs16942341(C;T) |
| Make rs16942341(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 88845674 |
| Gene | ACAN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16942341 |
| dbSNP (classic) | rs16942341 |
| ClinGen | rs16942341 |
| ebi | rs16942341 |
| HLI | rs16942341 |
| Exac | rs16942341 |
| Gnomad | rs16942341 |
| Varsome | rs16942341 |
| LitVar | rs16942341 |
| Map | rs16942341 |
| PheGenI | rs16942341 |
| Biobank | rs16942341 |
| 1000 genomes | rs16942341 |
| hgdp | rs16942341 |
| ensembl | rs16942341 |
| geneview | rs16942341 |
| scholar | rs16942341 |
| rs16942341 | |
| pharmgkb | rs16942341 |
| gwascentral | rs16942341 |
| openSNP | rs16942341 |
| 23andMe | rs16942341 |
| SNPshot | rs16942341 |
| SNPdbe | rs16942341 |
| MSV3d | rs16942341 |
| GWAS Ctlg | rs16942341 |
| GMAF | 0.04591 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 4E-27 |
| Odds Ratio | .13 [NR] unit decrease |
