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rs11226373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11226373(A;G)
Make rs11226373(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position104463511
is asnp
is mentioned by
dbSNPrs11226373
ebirs11226373
HLIrs11226373
Exacrs11226373
Varsomers11226373
Maprs11226373
PheGenIrs11226373
hapmaprs11226373
1000 genomesrs11226373
hgdprs11226373
ensemblrs11226373
gopubmedrs11226373
geneviewrs11226373
scholarrs11226373
googlers11226373
pharmgkbrs11226373
gwascentralrs11226373
openSNPrs11226373
23andMers11226373
23andMe allrs11226373
SNP Nexus

SNPshotrs11226373
SNPdbers11226373
MSV3drs11226373
GWAS Ctlgrs11226373
GMAF0.1474
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20031604OA-icon.png]
Trait Serum Matrix Metalloproteinase
Title Genome-Wide Association Scan Identifies Variants near Matrix Metalloproteinase (MMP) Genes on Chromosome 11q21-22 Strongly Associated With Serum MMP-1 Levels
Risk Allele G
P-val 2E-18
Odds Ratio 0.44 [NR] unit increase in ln(MMP-1)



GET Evidence
rs11226373
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary