{{Rsnum
|rsid=6598163
|Gene=MMP17
|Chromosome=12
|position=131840694
|Orientation=plus
|GMAF=0.4642
|Gene_s=MMP17
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.8 | 47.2 | 25.0
| HCB | 34.3 | 41.8 | 23.9
| JPT | 14.7 | 48.6 | 36.7
| YRI | 19.4 | 52.8 | 27.8
| ASW | 18.5 | 48.1 | 33.3
| CHB | 34.3 | 41.8 | 23.9
| CHD | 22.0 | 52.3 | 25.7
| GIH | 12.1 | 48.5 | 39.4
| LWK | 18.2 | 55.5 | 26.4
| MEX | 19.3 | 47.4 | 33.3
| MKK | 26.3 | 48.7 | 25.0
| TSI | 20.0 | 49.0 | 31.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22683712
|Trait=None
|Title=Genome-wide association analysis identifies susceptibility loci for migraine without aura.
|RiskAllele=G
|Pval=5E-7
|OR=1.1500
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=MMP17
|aa_change=Ala182Thr
|aa_change_short=A182T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6598163
|overall_frequency_n=5028
|overall_frequency_d=10756
|overall_frequency=0.46746
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=52
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}