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1.

rs1695 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G,T [Show Flanks]
    Chromosome:
    11:67585218 (GRCh38)
    11:67352689 (GRCh37)
    Canonical SPDI:
    NC_000011.10:67585217:A:G,NC_000011.10:67585217:A:T
    Gene:
    GSTP1 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant
    Clinical significance:
    benign,not-provided
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.329091/121104 (ALFA)
    G=0.145331/11255 (TOMMO)
    G=0.183276/537 (KOREAN)
    G=0.183406/336 (Korea1K)
    G=0.185606/147 (PRJEB37584)
    G=0.187586/1357 (Korea4K)
    G=0.204082/20 (PRJEB36033)
    G=0.236928/145 (Vietnamese)
    G=0.244966/73 (FINRISK)
    G=0.275/11 (GENOME_DK)
    G=0.277778/60 (Qatari)
    G=0.278333/167 (NorthernSweden)
    G=0.290262/155 (MGP)
    G=0.299232/623 (HGDP_Stanford)
    G=0.31183/1397 (Estonian)
    G=0.323647/323 (GoNL)
    A=0.333333/10 (Siberian)
    G=0.333481/39957 (ExAC)
    G=0.344577/1328 (ALSPAC)
    G=0.345137/653 (HapMap)
    G=0.349515/1296 (TWINSUK)
    G=0.352636/1766 (1000Genomes)
    G=0.360037/53562 (GnomAD_genomes)
    G=0.360837/4535 (GoESP)
    G=0.362274/2320 (1000Genomes_30X)
    G=0.37384/403 (PharmGKB)
    A=0.378289/115 (SGDP_PRJ)
    G=0.379663/100493 (TOPMED)
    G=0.39617/31177 (PAGE_STUDY)
    HGVS:

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