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1.

rs1721312444 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>T [Show Flanks]
    Chromosome:
    3:197974429 (GRCh38)
    3:197701300 (GRCh37)
    Canonical SPDI:
    NC_000003.12:197974428:A:T
    Gene:
    LMLN (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,non_coding_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    T=0./0 (ALFA)
    T=0.000004/1 (TOPMED)
    HGVS:

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