rs205611
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs205611(A;A) |
| Make rs205611(A;G) |
| Make rs205611(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 74744954 |
| Gene | LOC102724497 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs205611 |
| dbSNP (classic) | rs205611 |
| ClinGen | rs205611 |
| ebi | rs205611 |
| HLI | rs205611 |
| Exac | rs205611 |
| Gnomad | rs205611 |
| Varsome | rs205611 |
| LitVar | rs205611 |
| Map | rs205611 |
| PheGenI | rs205611 |
| Biobank | rs205611 |
| 1000 genomes | rs205611 |
| hgdp | rs205611 |
| ensembl | rs205611 |
| geneview | rs205611 |
| scholar | rs205611 |
| rs205611 | |
| pharmgkb | rs205611 |
| gwascentral | rs205611 |
| openSNP | rs205611 |
| 23andMe | rs205611 |
| SNPshot | rs205611 |
| SNPdbe | rs205611 |
| MSV3d | rs205611 |
| GWAS Ctlg | rs205611 |
| GMAF | 0.09504 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21835309 |
| Trait | |
| Title | GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. |
| Risk Allele | A |
| P-val | 0.000001 |
| Odds Ratio | 0.1200 [0.06-0.18] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- 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
