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1.

rs28944221 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    17:27756374 (GRCh38)
    17:26083400 (GRCh37)
    Canonical SPDI:
    NC_000017.11:27756373:G:A
    Gene:
    NOS2 (Varview)
    Functional Consequence:
    downstream_transcript_variant,500B_downstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.011406/172 (ALFA)
    A=0.000013/1 (TOMMO)
    A=0.000259/1 (ALSPAC)
    A=0.00027/1 (TWINSUK)
    A=0.009259/2 (Qatari)
    A=0.015402/2299 (GnomAD_genomes)
    A=0.016457/4356 (TOPMED)
    A=0.017772/89 (1000Genomes)
    A=0.018114/116 (1000Genomes_30X)
    A=0.024626/1938 (PAGE_STUDY)
    G=0.4375/7 (SGDP_PRJ)
    HGVS:

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