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1.

rs17174829 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    6:154091128 (GRCh38)
    6:154412263 (GRCh37)
    Canonical SPDI:
    NC_000006.12:154091127:G:A
    Gene:
    OPRM1 (Varview)
    Functional Consequence:
    intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.0002546/54 (ALFA)
    A=0./0 (ALSPAC)
    A=0.0000381/3 (PAGE_STUDY)
    A=0.0001407/21 (GnomAD_genomes)
    A=0.0001408/17 (ExAC)
    A=0.0001511/40 (TOPMED)
    A=0.0001562/1 (1000Genomes_30X)
    A=0.0001997/1 (1000Genomes)
    A=0.0002697/1 (TWINSUK)
    A=0.0002897/406 (GnomAD_exomes)
    A=0.0003848/5 (GoESP)
    A=0.0021277/7 (PRJEB37766)
    A=0.004008/4 (GoNL)
    A=0.0056818/3 (HapMap)
    HGVS:
    NC_000006.12:g.154091128G>A, NC_000006.11:g.154412263G>A, NG_021208.2:g.85628G>A, NM_000914.5:c.820G>A, NM_000914.4:c.820G>A, NM_000914.3:c.820G>A, NM_001145279.4:c.1099G>A, NM_001145279.3:c.1099G>A, NM_001145279.2:c.1099G>A, NM_001145280.4:c.520G>A, NM_001145280.3:c.520G>A, NM_001145280.2:c.520G>A, NM_001008504.4:c.820G>A, NM_001008504.3:c.820G>A, NM_001008504.2:c.820G>A, NM_001145287.3:c.520G>A, NM_001145287.2:c.520G>A, NM_001145287.1:c.520G>A, NM_001145281.3:c.577G>A, NM_001145281.2:c.577G>A, NM_001145281.1:c.577G>A, NM_001145284.3:c.820G>A, NM_001145284.2:c.820G>A, NM_001145286.3:c.820G>A, NM_001145286.2:c.820G>A, NM_001145286.1:c.820G>A, NM_001008503.3:c.820G>A, NM_001008503.2:c.820G>A, NM_001008503.1:c.820G>A, NM_001285523.3:c.820G>A, NM_001285523.2:c.820G>A, NM_001285523.1:c.820G>A, NM_001145285.3:c.820G>A, NM_001145285.2:c.820G>A, NM_001145285.1:c.820G>A, NM_001285526.2:c.520G>A, NM_001285526.1:c.520G>A, NM_001145283.2:c.820G>A, NM_001145283.1:c.820G>A, NM_001008505.2:c.820G>A, NM_001008505.1:c.820G>A, NM_001145282.2:c.820G>A, NM_001145282.1:c.820G>A, NM_001285528.2:c.520G>A, NM_001285528.1:c.520G>A, NM_001285524.1:c.1099G>A, NR_104348.1:n.954G>A, NR_104350.1:n.601G>A, NR_104351.1:n.954G>A, NR_104349.1:n.954G>A, NM_001285527.1:c.520G>A, XM_011535851.4:c.520G>A, XM_011535851.3:c.520G>A, XM_011535851.2:c.520G>A, XM_011535851.1:c.520G>A, XM_017010903.3:c.520G>A, XM_017010903.2:c.520G>A, XM_017010903.1:c.520G>A, XM_011535853.3:c.520G>A, XM_011535853.2:c.520G>A, XM_011535853.1:c.520G>A, XM_011535862.3:c.520G>A, XM_011535862.2:c.520G>A, XM_011535862.1:c.520G>A, XM_011535856.3:c.520G>A, XM_011535856.2:c.520G>A, XM_011535856.1:c.520G>A, XM_017010904.2:c.520G>A, XM_017010904.1:c.520G>A, NP_000905.3:p.Asp274Asn, NP_001138751.1:p.Asp367Asn, NP_001138752.1:p.Asp174Asn, NP_001008504.2:p.Asp274Asn, NP_001138759.1:p.Asp174Asn, NP_001138753.1:p.Asp193Asn, NP_001138756.1:p.Asp274Asn, NP_001138758.1:p.Asp274Asn, NP_001008503.2:p.Asp274Asn, NP_001272452.1:p.Asp274Asn, NP_001138757.1:p.Asp274Asn, NP_001272455.1:p.Asp174Asn, NP_001138755.1:p.Asp274Asn, NP_001008505.2:p.Asp274Asn, NP_001138754.1:p.Asp274Asn, NP_001272457.1:p.Asp174Asn, NP_001272453.1:p.Asp367Asn, NP_001272456.1:p.Asp174Asn, XP_011534153.1:p.Asp174Asn, XP_016866392.1:p.Asp174Asn, XP_011534155.1:p.Asp174Asn, XP_011534164.1:p.Asp174Asn, XP_011534158.1:p.Asp174Asn, XP_016866393.1:p.Asp174Asn

    PubMed

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