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1.

rs5859170 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ACA>-,ACAACA [Show Flanks]
    Chromosome:
    4:69285526 (GRCh38)
    4:70151244 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69285522:ACAACA:ACA,NC_000004.12:69285522:ACAACA:ACAACAACA
    Gene:
    UGT2B28 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ACAACAACA=0.009087/143 (ALFA)
    -=0.000004/1 (TOPMED)
    ACA=0.014976/75 (1000Genomes)
    -=0.022044/22 (GoNL)
    -=0.027119/16 (NorthernSweden)
    HGVS:

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