NC_000019.10:g.33829547=

HGVS Expressions

  • NC_000019.10:g.33829547=
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Variant Type

Reference Allele

dbSNP

368794

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601665.G.3.1United Arab Emirates2510.401ObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates3070.396El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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