rs6747972
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6747972(A;A) |
Make rs6747972(A;G) |
Make rs6747972(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 67843093 |
is a | snp |
is | mentioned by |
dbSNP | rs6747972 |
dbSNP (classic) | rs6747972 |
ClinGen | rs6747972 |
ebi | rs6747972 |
HLI | rs6747972 |
Exac | rs6747972 |
Gnomad | rs6747972 |
Varsome | rs6747972 |
LitVar | rs6747972 |
Map | rs6747972 |
PheGenI | rs6747972 |
Biobank | rs6747972 |
1000 genomes | rs6747972 |
hgdp | rs6747972 |
ensembl | rs6747972 |
geneview | rs6747972 |
scholar | rs6747972 |
rs6747972 | |
pharmgkb | rs6747972 |
gwascentral | rs6747972 |
openSNP | rs6747972 |
23andMe | rs6747972 |
SNPshot | rs6747972 |
SNPdbe | rs6747972 |
MSV3d | rs6747972 |
GWAS Ctlg | rs6747972 |
GMAF | 0.3444 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21779176] |
Trait | |
Title | Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. |
Risk Allele | A |
P-val | 9E-11 |
Odds Ratio | 1.2300 [1.16-1.31] |