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1.

rs35527513 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    C>- [Show Flanks]
    Chromosome:
    6:126689325 (GRCh38)
    6:127010470 (GRCh37)
    Canonical SPDI:
    NC_000006.12:126689324:CCC:CC
    Gene:
    LOC105377992 (Varview)
    Functional Consequence:
    genic_upstream_transcript_variant,intron_variant
    HGVS:

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