NC_000018.10:g.3043518T>C

HGVS Expressions

  • NC_000018.10:g.3043518T>C
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Variant Type

Substitution

dbSNP

4528660

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.5United Arab Emirates0.178Osman et al. 2018 115 patients with T2DM
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