rs4900109
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4900109(G;G) |
Make rs4900109(G;T) |
Make rs4900109(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 92297047 |
is a | snp |
is | mentioned by |
dbSNP | rs4900109 |
dbSNP (classic) | rs4900109 |
ClinGen | rs4900109 |
ebi | rs4900109 |
HLI | rs4900109 |
Exac | rs4900109 |
Gnomad | rs4900109 |
Varsome | rs4900109 |
LitVar | rs4900109 |
Map | rs4900109 |
PheGenI | rs4900109 |
Biobank | rs4900109 |
1000 genomes | rs4900109 |
hgdp | rs4900109 |
ensembl | rs4900109 |
geneview | rs4900109 |
scholar | rs4900109 |
rs4900109 | |
pharmgkb | rs4900109 |
gwascentral | rs4900109 |
openSNP | rs4900109 |
23andMe | rs4900109 |
SNPshot | rs4900109 |
SNPdbe | rs4900109 |
MSV3d | rs4900109 |
GWAS Ctlg | rs4900109 |
GMAF | 0.2934 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 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 | G |
P-val | 8E-21 |
Odds Ratio | 0.1700 [0.13-0.21] unit increase |