NM_001003760.4:c.*1266=

HGVS Expressions

  • NM_001003760.4:c.*1266=
  • NP_001003760.2:p.?
  • NC_000006.12:g.53650332=

Associated Genes

Kelch-Like 31
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Variant Type

Reference Allele

dbSNP

6941645

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 Emirates0.059Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.024Osman et al. 2020b 104 control subjects
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