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