rs6699417
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6699417(C;C) |
| Make rs6699417(C;T) |
| Make rs6699417(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 88657760 |
| Gene | PKN2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6699417 |
| dbSNP (classic) | rs6699417 |
| ClinGen | rs6699417 |
| ebi | rs6699417 |
| HLI | rs6699417 |
| Exac | rs6699417 |
| Gnomad | rs6699417 |
| Varsome | rs6699417 |
| LitVar | rs6699417 |
| Map | rs6699417 |
| PheGenI | rs6699417 |
| Biobank | rs6699417 |
| 1000 genomes | rs6699417 |
| hgdp | rs6699417 |
| ensembl | rs6699417 |
| geneview | rs6699417 |
| scholar | rs6699417 |
| rs6699417 | |
| pharmgkb | rs6699417 |
| gwascentral | rs6699417 |
| openSNP | rs6699417 |
| 23andMe | rs6699417 |
| SNPshot | rs6699417 |
| SNPdbe | rs6699417 |
| MSV3d | rs6699417 |
| GWAS Ctlg | rs6699417 |
| GMAF | 0.3889 |
| 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 | 5E-9 |
| Odds Ratio | 0.0200 [NR] meters increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- 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
