NM_021943.2:c.530-12146T>C

HGVS Expressions

  • NM_021943.2:c.530-12146T>C
  • NP_068762.1:p.?
  • NC_000006.12:g.38140089T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.32.3United Arab EmiratesNA0.075AssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
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