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1.

rs1724861 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    2:149762276 (GRCh38)
    2:150618790 (GRCh37)
    Canonical SPDI:
    NC_000002.12:149762275:A:G
    Gene:
    MMADHC-DT (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.231958/4294 (ALFA)
    G=0.018823/55 (KOREAN)
    G=0.020197/37 (Korea1K)
    G=0.021018/152 (Korea4K)
    G=0.023592/1827 (TOMMO)
    G=0.06513/65 (GoNL)
    G=0.180556/39 (Qatari)
    G=0.195288/978 (1000Genomes)
    G=0.198314/1270 (1000Genomes_30X)
    G=0.205054/917 (Estonian)
    G=0.225/9 (GENOME_DK)
    G=0.226667/136 (NorthernSweden)
    G=0.230145/33888 (GnomAD_genomes)
    G=0.230912/61120 (TOPMED)
    A=0.409091/81 (SGDP_PRJ)
    HGVS:

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