--- 
- 
  allele_string: T/A/C
  assembly_name: GRCh38
  colocated_variants: 
    - 
      allele_string: T/A/C
      end: 99451590
      frequencies: 
        A: 
          gnomadg: '6.597e-06'
          gnomadg_afr: '2.423e-05'
          gnomadg_ami: 0
          gnomadg_amr: 0
          gnomadg_asj: 0
          gnomadg_eas: 0
          gnomadg_fin: 0
          gnomadg_mid: 0
          gnomadg_nfe: 0
          gnomadg_remaining: 0
          gnomadg_sas: 0
        C: 
          af: '0.521'
          afr: '0.3502'
          amr: '0.4856'
          eas: '0.6786'
          eur: '0.495'
          gnomadg: '0.4891'
          gnomadg_afr: '0.377'
          gnomadg_ami: '0.4736'
          gnomadg_amr: '0.4608'
          gnomadg_asj: '0.4473'
          gnomadg_eas: '0.6475'
          gnomadg_fin: '0.5898'
          gnomadg_mid: '0.4252'
          gnomadg_nfe: '0.5321'
          gnomadg_remaining: '0.441'
          gnomadg_sas: '0.6088'
          sas: '0.6411'
      id: rs2656176
      seq_region_name: 11
      start: 99451590
      strand: 1
  end: 99451590
  id: rs2656176
  input: rs2656176
  most_severe_consequence: intron_variant
  seq_region_name: 11
  start: 99451590
  strand: 1
  transcript_consequences: 
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000524871
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000524871
      variant_allele: C
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000527185
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000527185
      variant_allele: C
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000528682
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000528682
      variant_allele: C
    - 
      biotype: retained_intron
      consequence_terms: 
        - intron_variant
        - non_coding_transcript_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000528727
      variant_allele: A
    - 
      biotype: retained_intron
      consequence_terms: 
        - intron_variant
        - non_coding_transcript_variant
      gene_id: ENSG00000149972
      gene_symbol: CNTN5
      gene_symbol_source: HGNC
      hgnc_id: HGNC:2175
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000528727
      variant_allele: C