NM_182575.3:c.235+152=

HGVS Expressions

  • NM_182575.3:c.235+152=
  • NP_001308793.1:p.?
  • NC_000019.10:g.48745473=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

838145

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
609436.G.1United Arab Emirates280.27AssociationSaber-Ayad et al. 2020 Presence of AA genotype of rs838133 (alt...
609436.G.2United Arab Emirates1820.47Naja et al. 2021 Participants carrying the A allele were ...
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