NM_001278293.3:c.535+80A>G

HGVS Expressions

  • NG_008119.2:g.32156A>G
  • NM_001278293.3:c.535+80A>G
  • NC_000003.12:g.97791906A>G
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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
209900.9.1Saudi Arabia1BenignAbu-Safieh et al. 2012; Abu Safieh et al. 2010 "BBS-F026-A" in the publication
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