NM_030923.4:c.322+39078T>G

HGVS Expressions

  • NM_030923.4:c.322+39078T>G
  • NP_112185.1:p.?
  • NC_000002.12:g.134674122A>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4954160

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.32.3United Arab EmiratesNA0.196AssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
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