NC_000002.12:g.111192964T>C

HGVS Expressions

  • NC_000002.12:g.111192964T>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 EmiratesNA0.481AssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
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