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rs20544

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs20544(C;T)
Make rs20544(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position46016371
GeneMMP9
is asnp
is mentioned by
dbSNPrs20544
dbSNP (old)rs20544
ClinGenrs20544
ebirs20544
HLIrs20544
Exacrs20544
Varsomers20544
Maprs20544
PheGenIrs20544
Biobankrs20544
1000 genomesrs20544
hgdprs20544
ensemblrs20544
gopubmedrs20544
geneviewrs20544
scholarrs20544
googlers20544
pharmgkbrs20544
gwascentralrs20544
openSNPrs20544
23andMers20544
23andMe allrs20544
SNP Nexus

SNPshotrs20544
SNPdbers20544
MSV3drs20544
GWAS Ctlgrs20544
GMAF0.2805
Max Magnitude0

[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


[PMID 20078883OA-icon.png] Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.


ClinVar
Risk rs20544(T;T)
Alt rs20544(T;T)
Reference Rs20544(C;C)
Significance Non-pathogenic
Disease Metaphyseal anadysplasia
Variation info
Gene MMP9
CLNDBN Metaphyseal anadysplasia
Reversed 0
HGVS NC_000020.10:g.44645010C>T
CLNSRC
CLNACC RCV000286736.1,