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rs7217186

From SNPedia

Orientationplus
Stabilizedplus
Make rs7217186(C;C)
Make rs7217186(C;T)
Make rs7217186(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4636097
GeneALOX15
is asnp
is mentioned by
dbSNPrs7217186
ebirs7217186
HLIrs7217186
Exacrs7217186
Varsomers7217186
Maprs7217186
PheGenIrs7217186
hapmaprs7217186
1000 genomesrs7217186
hgdprs7217186
ensemblrs7217186
gopubmedrs7217186
geneviewrs7217186
scholarrs7217186
googlers7217186
pharmgkbrs7217186
gwascentralrs7217186
openSNPrs7217186
23andMers7217186
23andMe allrs7217186
SNP Nexus

SNPshotrs7217186
SNPdbers7217186
MSV3drs7217186
GWAS Ctlgrs7217186
GMAF0.4729
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20676957] Two single nucleotide polymorphisms in ALOX15 are associated with risk of coronary artery disease in a Chinese Han population


[PMID 22351111] Association of ALOX15 gene polymorphism with ischemic stroke in Northern Chinese Han population.