NC_000001.11:g.72346757=

HGVS Expressions

  • NC_000001.11:g.72346757=
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Variant Type

Reference Allele

dbSNP

2815752

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 Emirates1710.272ObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates2480.319El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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