NR_002832.2:n.375-4076=

HGVS Expressions

  • NG_011794.1:g.72892=
  • NR_002832.2:n.375-4076=
  • NC_000011.10:g.27654165=
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Variant Type

Reference Allele

dbSNP

1519480

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605552.G.3.1United Arab Emirates0.339Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.255Osman et al. 2020b 104 control subjects
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