NM_198428.3:c.1693+102G>A

HGVS Expressions

  • NG_009306.2:g.233854G>A
  • NM_198428.3:c.1693+102G>A
  • NP_940820.1:p.?
  • NC_000007.14:g.33358097G>A
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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 Arabia1BenignAbu-Safieh et al. 2012 "BBS-F031-A" in the publication
615983.3United Arab Emirates1BenignAbu-Safieh et al. 2012 "BBS-F030-A" in the publication
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