rs56216945
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs56216945(A;A) |
Make rs56216945(A;G) |
Make rs56216945(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 35779997 |
Gene | LOC105374724, SPEF2 |
is a | snp |
is | mentioned by |
dbSNP | rs56216945 |
dbSNP (classic) | rs56216945 |
ClinGen | rs56216945 |
ebi | rs56216945 |
HLI | rs56216945 |
Exac | rs56216945 |
Gnomad | rs56216945 |
Varsome | rs56216945 |
LitVar | rs56216945 |
Map | rs56216945 |
PheGenI | rs56216945 |
Biobank | rs56216945 |
1000 genomes | rs56216945 |
hgdp | rs56216945 |
ensembl | rs56216945 |
geneview | rs56216945 |
scholar | rs56216945 |
rs56216945 | |
pharmgkb | rs56216945 |
gwascentral | rs56216945 |
openSNP | rs56216945 |
23andMe | rs56216945 |
SNPshot | rs56216945 |
SNPdbe | rs56216945 |
MSV3d | rs56216945 |
GWAS Ctlg | rs56216945 |
Max Magnitude | 0 |
[PMID 29285564] The effects of CXCL10 polymorphisms on COPD susceptibility.