NM_006311.4:c.242+4879GT[2]

HGVS Expressions

  • NG_047111.1:g.40072GT[2]
  • NM_006311.4:c.242+4879GT[2]
  • NC_000017.11:g.16181672AC[2]
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Variant Type

Microsatellite

dbSNP

1305047

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.555Almheiri et al. 2019 500 healthy Emiratis (254 females)
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