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1.

rs1137070 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    X:43744144 (GRCh38)
    X:43603391 (GRCh37)
    Canonical SPDI:
    NC_000023.11:43744143:T:C
    Gene:
    MAOA (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.310157/88301 (ALFA)
    T=0.129944/46 (SGDP_PRJ)
    T=0.2/8 (GENOME_DK)
    T=0.235294/8 (Siberian)
    T=0.2603/139 (MGP)
    T=0.29288/1086 (TWINSUK)
    T=0.300796/869 (ALSPAC)
    T=0.314815/34 (Qatari)
    T=0.326801/3452 (GoESP)
    T=0.349144/92415 (TOPMED)
    T=0.374031/32470 (ExAC)
    T=0.404511/843 (HGDP_Stanford)
    C=0.408673/27039 (TOMMO)
    C=0.418919/62 (Vietnamese)
    T=0.428571/24 (PRJEB36033)
    T=0.431674/815 (HapMap)
    C=0.436649/2278 (Korea4K)
    T=0.440791/2118 (1000Genomes_30X)
    T=0.441011/157 (PharmGKB)
    C=0.445734/1306 (KOREAN)
    T=0.448212/1692 (1000Genomes)
    HGVS:

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