NC_000011.10:g.2191936C>T

HGVS Expressions

  • NC_000011.10:g.2191936C>T
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CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

7111341

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 EmiratesNA0.185AssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
222100.G.5.1United Arab Emirates490.176BenignSharma et al. 2021 139 patients with Type I diabetes. Signi...
222100.G.5.2United Arab Emirates540.158BenignSharma et al. 2021 171 healthy controls
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