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1.

rs13306584 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A,C,G [Show Flanks]
    Chromosome:
    5:143399587 (GRCh38)
    5:142779152 (GRCh37)
    Canonical SPDI:
    NC_000005.10:143399586:T:A,NC_000005.10:143399586:T:C,NC_000005.10:143399586:T:G
    Gene:
    NR3C1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.00004/1 (ALFA)
    C=0./0 (HapMap)
    C=0.000991/148 (GnomAD_genomes)
    C=0.00609/39 (1000Genomes_30X)
    C=0.00639/32 (1000Genomes)
    C=0.012139/940 (TOMMO)
    C=0.015348/111 (Korea4K)
    C=0.0154/45 (KOREAN)
    C=0.017467/32 (Korea1K)
    C=0.018519/4 (Vietnamese)
    T=0.5/2 (SGDP_PRJ)
    HGVS:

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