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rs56216945

From SNPedia

Orientationplus
Stabilizedplus
Make rs56216945(A;A)
Make rs56216945(A;G)
Make rs56216945(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position35779997
GeneLOC105374724, SPEF2
is asnp
is mentioned by
dbSNPrs56216945
dbSNP (classic)rs56216945
ClinGenrs56216945
ebirs56216945
HLIrs56216945
Exacrs56216945
Gnomadrs56216945
Varsomers56216945
LitVarrs56216945
Maprs56216945
PheGenIrs56216945
Biobankrs56216945
1000 genomesrs56216945
hgdprs56216945
ensemblrs56216945
geneviewrs56216945
scholarrs56216945
googlers56216945
pharmgkbrs56216945
gwascentralrs56216945
openSNPrs56216945
23andMers56216945
SNPshotrs56216945
SNPdbers56216945
MSV3drs56216945
GWAS Ctlgrs56216945
Max Magnitude0

[PMID 29285564] The effects of CXCL10 polymorphisms on COPD susceptibility.