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1.

rs4328 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    17:63486052 (GRCh38)
    17:61563413 (GRCh37)
    Canonical SPDI:
    NC_000017.11:63486051:T:C
    Gene:
    ACE (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.026586/756 (ALFA)
    C=0./0 (TWINSUK)
    C=0.000519/2 (ALSPAC)
    C=0.013889/3 (Qatari)
    C=0.034462/5144 (GnomAD_genomes)
    C=0.03754/188 (1000Genomes)
    C=0.03935/252 (1000Genomes_30X)
    C=0.039975/10581 (TOPMED)
    C=0.074468/14 (PharmGKB)
    T=0.4/4 (SGDP_PRJ)
    HGVS:

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