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1.

rs10989589 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    9:101670953 (GRCh38)
    9:104433235 (GRCh37)
    Canonical SPDI:
    NC_000009.12:101670952:C:T
    Gene:
    GRIN3A (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.391039/92774 (ALFA)
    T=0.165539/12820 (TOMMO)
    T=0.1735808/318 (Korea1K)
    T=0.1886062/1364 (Korea4K)
    T=0.1940452/567 (KOREAN)
    T=0.2126582/168 (PRJEB37584)
    T=0.2195122/72 (HapMap)
    T=0.2537068/154 (Vietnamese)
    T=0.2581194/20314 (PAGE_STUDY)
    T=0.261243/1673 (1000Genomes_30X)
    T=0.2653754/1329 (1000Genomes)
    T=0.3255544/86171 (TOPMED)
    T=0.3298478/4290 (GoESP)
    T=0.3311152/49311 (GnomAD_genomes)
    T=0.3585526/109 (FINRISK)
    T=0.3596598/43644 (ExAC)
    T=0.3703704/80 (Qatari)
    T=0.375/15 (GENOME_DK)
    T=0.3827655/382 (GoNL)
    T=0.3873239/440 (Daghestan)
    C=0.3885135/115 (SGDP_PRJ)
    T=0.389785/546148 (GnomAD_exomes)
    T=0.3972496/1531 (ALSPAC)
    T=0.4050701/1502 (TWINSUK)
    C=0.4285714/12 (Siberian)
    T=0.4475655/239 (MGP)
    T=0.4651786/2084 (Estonian)
    T=0.4783333/287 (NorthernSweden)
    HGVS:

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