rs1474563
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1474563(C;C) |
| Make rs1474563(C;T) |
| Make rs1474563(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 79393696 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1474563 |
| dbSNP (classic) | rs1474563 |
| ClinGen | rs1474563 |
| ebi | rs1474563 |
| HLI | rs1474563 |
| Exac | rs1474563 |
| Gnomad | rs1474563 |
| Varsome | rs1474563 |
| LitVar | rs1474563 |
| Map | rs1474563 |
| PheGenI | rs1474563 |
| Biobank | rs1474563 |
| 1000 genomes | rs1474563 |
| hgdp | rs1474563 |
| ensembl | rs1474563 |
| geneview | rs1474563 |
| scholar | rs1474563 |
| rs1474563 | |
| pharmgkb | rs1474563 |
| gwascentral | rs1474563 |
| openSNP | rs1474563 |
| 23andMe | rs1474563 |
| SNPshot | rs1474563 |
| SNPdbe | rs1474563 |
| MSV3d | rs1474563 |
| GWAS Ctlg | rs1474563 |
| GMAF | 0.3579 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | T |
| P-val | 0.0000030000000000000001 |
| Odds Ratio | 3.50 [1.93-5.07] % SD taller |
[PMID 21253569
] Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome X
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
