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1.

rs1136410 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G,T [Show Flanks]
    Chromosome:
    1:226367601 (GRCh38)
    1:226555302 (GRCh37)
    Canonical SPDI:
    NC_000001.11:226367600:A:C,NC_000001.11:226367600:A:G,NC_000001.11:226367600:A:T
    Gene:
    PARP1 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.1650951/63520 (ALFA)
    G=0.1179775/63 (MGP)
    G=0.1233277/1604 (GoESP)
    G=0.1435185/31 (Qatari)
    G=0.1467098/544 (TWINSUK)
    G=0.1577158/23523 (GnomAD_genomes)
    G=0.1587961/612 (ALSPAC)
    G=0.1621104/42909 (TOPMED)
    G=0.1632653/16 (PRJEB36033)
    G=0.1692141/237118 (GnomAD_exomes)
    G=0.1804233/341 (HapMap)
    G=0.1823661/817 (Estonian)
    G=0.1923848/192 (GoNL)
    G=0.1962836/1257 (1000Genomes_30X)
    G=0.196885/986 (1000Genomes)
    G=0.2017787/24481 (ExAC)
    G=0.2030245/15976 (PAGE_STUDY)
    G=0.2302632/70 (FINRISK)
    G=0.2461612/513 (HGDP_Stanford)
    G=0.25/10 (GENOME_DK)
    G=0.2683333/161 (NorthernSweden)
    G=0.2827476/177 (Chileans)
    A=0.3846154/90 (SGDP_PRJ)
    G=0.402017/31133 (TOMMO)
    G=0.4198473/330 (PRJEB37584)
    G=0.4381107/269 (Vietnamese)
    G=0.4501706/1319 (KOREAN)
    G=0.4552402/834 (Korea1K)
    G=0.4559027/3298 (Korea4K)
    A=0.4583333/11 (Siberian)
    HGVS:

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