NM_144596.4:c.710+75G>C

HGVS Expressions

  • NG_008126.2:g.33979G>C
  • NM_144596.4:c.710+75G>C
  • NC_000014.9:g.88853131G>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
615982.6Saudi ArabiaBenignAbu-Safieh et al. 2012 "BBS-F031-A" in the publication
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