rs56218866
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs56218866(A;A) |
Make rs56218866(A;G) |
Make rs56218866(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 15 |
Position | 78629887 |
Gene | CHRNB4 |
is a | snp |
is | mentioned by |
dbSNP | rs56218866 |
dbSNP (classic) | rs56218866 |
ClinGen | rs56218866 |
ebi | rs56218866 |
HLI | rs56218866 |
Exac | rs56218866 |
Gnomad | rs56218866 |
Varsome | rs56218866 |
LitVar | rs56218866 |
Map | rs56218866 |
PheGenI | rs56218866 |
Biobank | rs56218866 |
1000 genomes | rs56218866 |
hgdp | rs56218866 |
ensembl | rs56218866 |
geneview | rs56218866 |
scholar | rs56218866 |
rs56218866 | |
pharmgkb | rs56218866 |
gwascentral | rs56218866 |
openSNP | rs56218866 |
23andMe | rs56218866 |
SNPshot | rs56218866 |
SNPdbe | rs56218866 |
MSV3d | rs56218866 |
GWAS Ctlg | rs56218866 |
Max Magnitude | 0 |
[PMID 27462996] An efficient method to genotype the polymorphisms of cholinergic nicotinic receptor subunit genes and their associations with COPD onset risk.