NM_019113.4:c.36=

HGVS Expressions

  • NG_033945.1:g.5186=
  • NM_019113.4:c.36=
  • NP_061986.1:p.Gly12=
  • NC_000019.10:g.48756272=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

838133

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
609436.G.1United Arab Emirates940.30AssociationSaber-Ayad et al. 2020 Presence of AA genotype of rs838133 (alt...
609436.G.2United Arab Emirates1150.32AssociationNaja et al. 2021 Participants carrying the A allele were ...
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