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1.

rs893584 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G [Show Flanks]
    Chromosome:
    9:84676077 (GRCh38)
    9:87290992 (GRCh37)
    Canonical SPDI:
    NC_000009.12:84676076:A:C,NC_000009.12:84676076:A:G
    Gene:
    NTRK2 (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.482228/4857 (ALFA)
    A=0.293991/137 (SGDP_PRJ)
    A=0.370307/1085 (KOREAN)
    A=0.38817/1739 (Estonian)
    A=0.392116/2835 (Korea4K)
    A=0.395833/19 (Siberian)
    A=0.404435/2590 (1000Genomes_30X)
    A=0.407407/88 (Vietnamese)
    A=0.407548/2041 (1000Genomes)
    A=0.413333/248 (NorthernSweden)
    A=0.414509/1537 (TWINSUK)
    A=0.41712/62145 (GnomAD_genomes)
    A=0.421206/111489 (TOPMED)
    A=0.422124/32691 (TOMMO)
    A=0.425926/92 (Qatari)
    A=0.428646/1652 (ALSPAC)
    A=0.429878/141 (HapMap)
    A=0.442886/442 (GoNL)
    A=0.475/19 (GENOME_DK)
    HGVS:

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