NM_001846.2:c.99+473=

HGVS Expressions

  • NG_032137.1:g.6313=
  • NM_001846.2:c.99+473=
  • NP_001837.2:p.?
  • NC_000013.11:g.110308596=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

3809346

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNA0.457AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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