NC_000012.12:g.115114632A>G

HGVS Expressions

  • NC_000012.12:g.115114632A>G
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Variant Type

Substitution

dbSNP

35444

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 Emirates0.365Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.428Osman et al. 2020b 104 control subjects
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