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1.

rs368548578 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    3:197980472 (GRCh38)
    3:197707343 (GRCh37)
    Canonical SPDI:
    NC_000003.12:197980471:A:G
    Gene:
    LMLN (Varview)
    Functional Consequence:
    non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000014/2 (GnomAD)
    G=0.000019/5 (TOPMED)
    G=0.000068/17 (GnomAD_exomes)
    G=0.000077/1 (GoESP)
    G=0.000082/10 (ExAC)
    G=0.000399/2 (1000Genomes)
    HGVS:

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