NM_001363894.1:c.46-40478T>A

HGVS Expressions

  • NG_012969.1:g.70700T>A
  • NM_001363894.1:c.46-40478T>A
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Genomic Location

chr16:53769662

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

1558902

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610966.G.1Lebanon2810.46Likely BenignNasreddine et al. 2019 308 Lebanese individuals; Average BMI= 2...
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