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rs10488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs10488(A;A)
Make rs10488(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position102797291
GeneMMP1, WTAPP1
is asnp
is mentioned by
dbSNPrs10488
dbSNP (classic)rs10488
ClinGenrs10488
ebirs10488
HLIrs10488
Exacrs10488
Gnomadrs10488
Varsomers10488
LitVarrs10488
Maprs10488
PheGenIrs10488
Biobankrs10488
1000 genomesrs10488
hgdprs10488
ensemblrs10488
geneviewrs10488
scholarrs10488
googlers10488
pharmgkbrs10488
gwascentralrs10488
openSNPrs10488
23andMers10488
SNPshotrs10488
SNPdbers10488
MSV3drs10488
GWAS Ctlgrs10488
GMAF0.07163
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23077567OA-icon.png] Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort


[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 rs10488(A;A)
Alt rs10488(A;A)
Reference Rs10488(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MMP1 WTAPP1
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.102668022C>T
CLNSRC
CLNACC RCV000454871.1,