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rs9509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9509(C;C)
Make rs9509(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position46016514
GeneMMP9
is asnp
is mentioned by
dbSNPrs9509
ClinGenrs9509
ebirs9509
HLIrs9509
Exacrs9509
Varsomers9509
Maprs9509
PheGenIrs9509
hapmaprs9509
1000 genomesrs9509
hgdprs9509
ensemblrs9509
gopubmedrs9509
geneviewrs9509
scholarrs9509
googlers9509
pharmgkbrs9509
gwascentralrs9509
openSNPrs9509
23andMers9509
23andMe allrs9509
SNP Nexus

SNPshotrs9509
SNPdbers9509
MSV3drs9509
GWAS Ctlgrs9509
GMAF0.1635
Max Magnitude0

[PMID 22796276] The rs9509 polymorphism of MMP-9 is associated with risk of hemorrhage in brain arteriovenous malformations


[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


ClinVar
Risk rs9509(C;C)
Alt rs9509(C;C)
Reference Rs9509(T;T)
Significance Non-pathogenic
Disease Metaphyseal anadysplasia
Variation info
Gene MMP9
CLNDBN Metaphyseal anadysplasia
Reversed 0
HGVS NC_000020.10:g.44645153T>C
CLNSRC
CLNACC RCV000341688.1,