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1.

rs4148752 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->TCTTT [Show Flanks]
    Chromosome:
    7:87513243 (GRCh38)
    7:87142560 (GRCh37)
    Canonical SPDI:
    NC_000007.14:87513243:CTTT:CTTTTCTTT
    Gene:
    ABCB1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    CTTT=0.394869/6449 (ALFA)
    -=0.35/14 (GENOME_DK)
    -=0.356184/2281 (1000Genomes_30X)
    -=0.359368/95121 (TOPMED)
    -=0.367412/1840 (1000Genomes)
    -=0.375035/2713 (Korea4K)
    -=0.375775/55741 (GnomAD_genomes)
    -=0.398416/30843 (TOMMO)
    -=0.4/240 (NorthernSweden)
    -=0.425852/425 (GoNL)
    -=0.429881/1594 (TWINSUK)
    -=0.432019/1665 (ALSPAC)
    -=0.439509/1969 (Estonian)
    HGVS:

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