NM_005959.3:c.223+5596C>G

HGVS Expressions

  • NG_028160.1:g.10922C>G
  • NM_005959.3:c.223+5596C>G
  • NP_005950.1:p.?
  • NC_000011.10:g.92975544C>G

Associated Genes

Melatonin Receptor 1B
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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.32.1United Arab EmiratesNA0.260AssociationType 2 Diabetes MellitusOsman et al. 2020 422 subjects with T2DM from a study cons...
125853.G.32.2United Arab EmiratesNA0.300Osman et al. 2020 Group consisting of 332 control subjects...
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