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Links from Gene

1.

rs893662 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    X:51683336 (GRCh38)
    X:51426269 (GRCh37)
    Canonical SPDI:
    NC_000023.11:51683335:A:G
    Gene:
    CENPVL2 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by cluster
    HGVS:

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