{{Rsnum
|rsid=1163662
|Gene=LIN7A
|Chromosome=12
|position=80898148
|Orientation=plus
|GMAF=0.3834
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LIN7A
}}{{PMID Auto
|PMID=20227257
|Title=Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians
|OA=1
}}

{{PharmGKB
|RSID=rs1163662
|Name_s=
|Gene_s=LIN7A
|Feature=
|Evidence=PubMed ID:20227257
|Annotation=Risk or phenotype-associated allele: Not specified. Phenotype: The strongest association with acute myocardial infarction was for this protective missense SNP (rs1163662) in the GP6 gene. Study size: 652 cases (acute myocardial infarction), 625 controls. Study population/ethnicity: white non-Hispanic men and women. Significance metric(s): OR = 0.70; Bonferroni-adjusted p < 0.05.
|Drugs=
|Drug Classes=
|Diseases=Myocardial Infarction
|Curation Level=Curated
|PharmGKB Accession ID=PA165291872
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1163662
|overall_frequency_n=67
|overall_frequency_d=118
|overall_frequency=0.567797
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=58
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}