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rs186021206

From SNPedia

Orientationplus
Stabilizedplus
Make rs186021206(A;A)
Make rs186021206(A;G)
Make rs186021206(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7166093
is asnp
is mentioned by
dbSNPrs186021206
dbSNP (old)rs186021206
ClinGenrs186021206
ebirs186021206
HLIrs186021206
Exacrs186021206
Gnomadrs186021206
Varsomers186021206
Maprs186021206
PheGenIrs186021206
Biobankrs186021206
1000 genomesrs186021206
hgdprs186021206
ensemblrs186021206
gopubmedrs186021206
geneviewrs186021206
scholarrs186021206
googlers186021206
pharmgkbrs186021206
gwascentralrs186021206
openSNPrs186021206
23andMers186021206
23andMe allrs186021206
SNP Nexus

SNPshotrs186021206
SNPdbers186021206
MSV3drs186021206
GWAS Ctlgrs186021206
Max Magnitude
This SNP is a proxy for the in/del variants discussed on the ASGR1 page; these variants are associated with lowered risk for myocardial infarction and coronary artery disease.