NC_000002.12:g.622827T>C

HGVS Expressions

  • NC_000002.12:g.622827T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2867125

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 Emirates5240.834AssociationObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates6200.796El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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