NM_198428.3:c.2522-33T>C

HGVS Expressions

  • NG_009306.2:g.480589T>C
  • NM_198428.3:c.2522-33T>C
  • NC_000007.14:g.33604832T>C
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CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615987.6.1Saudi Arabia1BenignStoetzel et al. 2006; Abu-Safieh et al. 2012 "BBS-F029-A" in the publication
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