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rs6747972

From SNPedia

Orientationplus
Stabilizedplus
Make rs6747972(A;A)
Make rs6747972(A;G)
Make rs6747972(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position67843093
is asnp
is mentioned by
dbSNPrs6747972
ebirs6747972
HLIrs6747972
Exacrs6747972
Varsomers6747972
Maprs6747972
PheGenIrs6747972
hapmaprs6747972
1000 genomesrs6747972
hgdprs6747972
ensemblrs6747972
gopubmedrs6747972
geneviewrs6747972
scholarrs6747972
googlers6747972
pharmgkbrs6747972
gwascentralrs6747972
openSNPrs6747972
23andMers6747972
23andMe allrs6747972
SNP Nexus

SNPshotrs6747972
SNPdbers6747972
MSV3drs6747972
GWAS Ctlgrs6747972
GMAF0.3444
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21779176OA-icon.png]
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]