rs7112925
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7112925(C;C) |
| Make rs7112925(C;T) |
| Make rs7112925(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 67058689 |
| Gene | RHOD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7112925 |
| dbSNP (classic) | rs7112925 |
| ClinGen | rs7112925 |
| ebi | rs7112925 |
| HLI | rs7112925 |
| Exac | rs7112925 |
| Gnomad | rs7112925 |
| Varsome | rs7112925 |
| LitVar | rs7112925 |
| Map | rs7112925 |
| PheGenI | rs7112925 |
| Biobank | rs7112925 |
| 1000 genomes | rs7112925 |
| hgdp | rs7112925 |
| ensembl | rs7112925 |
| geneview | rs7112925 |
| scholar | rs7112925 |
| rs7112925 | |
| pharmgkb | rs7112925 |
| gwascentral | rs7112925 |
| openSNP | rs7112925 |
| 23andMe | rs7112925 |
| SNPshot | rs7112925 |
| SNPdbe | rs7112925 |
| MSV3d | rs7112925 |
| GWAS Ctlg | rs7112925 |
| GMAF | 0.3448 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 9E-10 |
| Odds Ratio | 0.0200 [NR] meters decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- 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 HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
