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1.

rs1013457665 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    3:197999320 (GRCh38)
    3:197726191 (GRCh37)
    Canonical SPDI:
    NC_000003.12:197999319:C:T
    Gene:
    LMLN (Varview)
    Functional Consequence:
    non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.000028/1 (ALFA)
    T=0.000004/1 (TOPMED)
    T=0.000007/1 (GnomAD)
    HGVS:

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