NM_001080432.2:c.46-34805G>T

HGVS Expressions

  • NG_012969.1:g.76373G>T
  • NM_001080432.2:c.46-34805G>T
  • NP_001073901.1:p.?
  • NC_000016.10:g.53775335G>T
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1121980

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610966.G.4Lebanon2036BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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