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rs1057518391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518391(A;C)
Make rs1057518391(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position102948052
GeneMMP13
is asnp
is mentioned by
dbSNPrs1057518391
dbSNP (classic)rs1057518391
ClinGenrs1057518391
ebirs1057518391
HLIrs1057518391
Exacrs1057518391
Gnomadrs1057518391
Varsomers1057518391
LitVarrs1057518391
Maprs1057518391
PheGenIrs1057518391
Biobankrs1057518391
1000 genomesrs1057518391
hgdprs1057518391
ensemblrs1057518391
geneviewrs1057518391
scholarrs1057518391
googlers1057518391
pharmgkbrs1057518391
gwascentralrs1057518391
openSNPrs1057518391
23andMers1057518391
23andMe allrs1057518391
SNPshotrs1057518391
SNPdbers1057518391
MSV3drs1057518391
GWAS Ctlgrs1057518391
Max Magnitude0
ClinVar
Risk rs1057518391(C;C)
Alt rs1057518391(C;C)
Reference Rs1057518391(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MMP13
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.102818781T>G
CLNSRC
CLNACC RCV000414263.1,