rs186736700
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs186736700(A;A) |
Make rs186736700(A;C) |
Make rs186736700(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 68355058 |
is a | snp |
is | mentioned by |
dbSNP | rs186736700 |
dbSNP (classic) | rs186736700 |
ClinGen | rs186736700 |
ebi | rs186736700 |
HLI | rs186736700 |
Exac | rs186736700 |
Gnomad | rs186736700 |
Varsome | rs186736700 |
LitVar | rs186736700 |
Map | rs186736700 |
PheGenI | rs186736700 |
Biobank | rs186736700 |
1000 genomes | rs186736700 |
hgdp | rs186736700 |
ensembl | rs186736700 |
geneview | rs186736700 |
scholar | rs186736700 |
rs186736700 | |
pharmgkb | rs186736700 |
gwascentral | rs186736700 |
openSNP | rs186736700 |
23andMe | rs186736700 |
SNPshot | rs186736700 |
SNPdbe | rs186736700 |
MSV3d | rs186736700 |
GWAS Ctlg | rs186736700 |
Max Magnitude | 0 |
[PMID 29520036] Genome-wide analysis of insomnia disorder.: A meta-analysis including three ancestral groups and three study cohorts revealed a genome-wide significant locus on Chr 7 (q11.22); top SNP rs186736700, OR 0.607, p = 4.88 × 10e−9.