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rs1056628

From SNPedia

Orientationplus
Stabilizedplus
Make rs1056628(A;A)
Make rs1056628(A;C)
Make rs1056628(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position46016407
GeneMMP9, TRIM78P
is asnp
is mentioned by
dbSNPrs1056628
ebirs1056628
HLIrs1056628
Exacrs1056628
Varsomers1056628
Maprs1056628
PheGenIrs1056628
hapmaprs1056628
1000 genomesrs1056628
hgdprs1056628
ensemblrs1056628
gopubmedrs1056628
geneviewrs1056628
scholarrs1056628
googlers1056628
pharmgkbrs1056628
gwascentralrs1056628
openSNPrs1056628
23andMers1056628
23andMe allrs1056628
SNP Nexus

SNPshotrs1056628
SNPdbers1056628
MSV3drs1056628
GWAS Ctlgrs1056628
Max Magnitude

[PMID 23257658] A functional polymorphism at miR-491-5p binding site in the 3'-UTR of MMP-9 gene confers increased risk for atherosclerotic cerebral infarction in a Chinese population