NM_198353.2:c.961+36643G>A

HGVS Expressions

  • NM_198353.2:c.961+36643G>A
  • NP_938167.1:p.?
  • NC_000004.12:g.44410920C>T
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4695718

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.35.1United Arab EmiratesNA0.78Al Safar et al. 2013 Discovery GWAS group comprising 178 indi...
125853.G.35.2ArabNANAAssociationType 2 Diabetes MellitusAl Safar et al. 2013 Replication sample group comprising 315 ...
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