rs2145998
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2145998(A;A) |
| Make rs2145998(A;T) |
| Make rs2145998(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 79361940 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2145998 |
| dbSNP (classic) | rs2145998 |
| ClinGen | rs2145998 |
| ebi | rs2145998 |
| HLI | rs2145998 |
| Exac | rs2145998 |
| Gnomad | rs2145998 |
| Varsome | rs2145998 |
| LitVar | rs2145998 |
| Map | rs2145998 |
| PheGenI | rs2145998 |
| Biobank | rs2145998 |
| 1000 genomes | rs2145998 |
| hgdp | rs2145998 |
| ensembl | rs2145998 |
| geneview | rs2145998 |
| scholar | rs2145998 |
| rs2145998 | |
| pharmgkb | rs2145998 |
| gwascentral | rs2145998 |
| openSNP | rs2145998 |
| 23andMe | rs2145998 |
| SNPshot | rs2145998 |
| SNPdbe | rs2145998 |
| MSV3d | rs2145998 |
| GWAS Ctlg | rs2145998 |
| GMAF | 0.4578 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Risk Allele | A |
| P-val | 4E-13 |
| Odds Ratio | 0.03 [NR] unit decrease |
