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rs7872802

From SNPedia

Orientationplus
Stabilizedplus
Make rs7872802(A;A)
Make rs7872802(A;G)
Make rs7872802(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position129753451
GenePTGES
is asnp
is mentioned by
dbSNPrs7872802
ebirs7872802
HLIrs7872802
Exacrs7872802
Varsomers7872802
Maprs7872802
PheGenIrs7872802
hapmaprs7872802
1000 genomesrs7872802
hgdprs7872802
ensemblrs7872802
gopubmedrs7872802
geneviewrs7872802
scholarrs7872802
googlers7872802
pharmgkbrs7872802
gwascentralrs7872802
openSNPrs7872802
23andMers7872802
23andMe allrs7872802
SNP Nexus

SNPshotrs7872802
SNPdbers7872802
MSV3drs7872802
GWAS Ctlgrs7872802
GMAF0.2089
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population