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1.

rs1721838038 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    3:197990614 (GRCh38)
    3:197717485 (GRCh37)
    Canonical SPDI:
    NC_000003.12:197990613:G:A
    Gene:
    LMLN (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,non_coding_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    A=0./0 (ALFA)
    A=0.000004/1 (TOPMED)
    HGVS:

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