NM_000809.4:c.875-804A>G

HGVS Expressions

  • NG_011809.1:g.32531A>G
  • NM_000809.4:c.875-804A>G
  • NP_000800.2:p.?
  • NC_000004.12:g.46966033T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2055942

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 EmiratesNANAAl 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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