NM_003019.5:c.199+9G>A

HGVS Expressions

  • NG_042218.1:g.7654G>A
  • NM_003019.5:c.199+9G>A
  • NP_003010.4:p.?
  • NC_000010.11:g.79946452C>T
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Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

6413522

Clinvar

227074

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
178635.1United Arab Emirates1Alsamri et al. 2021 Article remark: "Individual screened for...
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