NM_001288706.1:c.-83-12074C>T

HGVS Expressions

  • NM_001288706.1:c.-83-12074C>T
  • NP_001275635.1:p.?
  • NC_000002.12:g.102141867C>T
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

2234650

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.3632BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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