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1.

rs13186575 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    5:21880534 (GRCh38)
    5:21880643 (GRCh37)
    Canonical SPDI:
    NC_000005.10:21880533:T:C
    Gene:
    CDH12 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.00017/2 (ALFA)
    C=0.00024/4 (GnomAD_genomes)
    HGVS:

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