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1.

rs1045642 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G,T [Show Flanks]
    Chromosome:
    7:87509329 (GRCh38)
    7:87138645 (GRCh37)
    Canonical SPDI:
    NC_000007.14:87509328:A:C,NC_000007.14:87509328:A:G,NC_000007.14:87509328:A:T
    Gene:
    ABCB1 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,synonymous_variant
    Clinical significance:
    drug-response,benign,not-provided,likely-benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.4970077/175893 (ALFA)
    A=0.3023256/130 (SGDP_PRJ)
    A=0.3341296/26296 (PAGE_STUDY)
    A=0.3366013/206 (Vietnamese)
    A=0.3421053/13 (Siberian)
    A=0.3488055/1022 (KOREAN)
    A=0.3642773/620 (HapMap)
    A=0.3740321/2705 (Korea4K)
    A=0.3841349/2460 (1000Genomes_30X)
    A=0.385101/305 (PRJEB37584)
    A=0.3951677/1979 (1000Genomes)
    A=0.3995633/732 (Korea1K)
    A=0.4008916/106112 (TOPMED)
    G=0.4116667/247 (NorthernSweden)
    G=0.4137324/470 (Daghestan)
    A=0.4219565/32678 (TOMMO)
    A=0.4233431/5506 (GoESP)
    A=0.4281772/63777 (GnomAD_genomes)
    A=0.4400749/235 (MGP)
    G=0.4440789/135 (FINRISK)
    G=0.4614347/1711 (TWINSUK)
    A=0.462963/100 (Qatari)
    G=0.4667878/1799 (ALSPAC)
    G=0.4680804/2097 (Estonian)
    G=0.4735028/663563 (GnomAD_exomes)
    G=0.4869739/486 (GoNL)
    A=0.4965641/60266 (ExAC)
    A=0.5/20 (GENOME_DK)
    HGVS:
    NC_000007.14:g.87509329A>C, NC_000007.14:g.87509329A>G, NC_000007.14:g.87509329A>T, NC_000007.13:g.87138645A>C, NC_000007.13:g.87138645A>G, NC_000007.13:g.87138645A>T, NG_011513.1:g.208920T>G, NG_011513.1:g.208920T>C, NG_011513.1:g.208920T>A, NM_000927.5:c.3435T>G, NM_000927.5:c.3435T>C, NM_000927.5:c.3435T>A, NM_000927.4:c.3435T>G, NM_000927.4:c.3435T>C, NM_000927.4:c.3435T>A, NM_001348945.2:c.3645T>G, NM_001348945.2:c.3645T>C, NM_001348945.2:c.3645T>A, NM_001348945.1:c.3645T>G, NM_001348945.1:c.3645T>C, NM_001348945.1:c.3645T>A, NM_001348944.2:c.3435T>G, NM_001348944.2:c.3435T>C, NM_001348944.2:c.3435T>A, NM_001348944.1:c.3435T>G, NM_001348944.1:c.3435T>C, NM_001348944.1:c.3435T>A, NM_001348946.2:c.3435T>G, NM_001348946.2:c.3435T>C, NM_001348946.2:c.3435T>A, NM_001348946.1:c.3435T>G, NM_001348946.1:c.3435T>C, NM_001348946.1:c.3435T>A, NP_000918.2:p.Ile1145Met, NP_001335874.1:p.Ile1215Met, NP_001335873.1:p.Ile1145Met, NP_001335875.1:p.Ile1145Met

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