NR_038264.1:n.469+40890C>T

HGVS Expressions

  • NR_038264.1:n.469+40890C>T
  • NC_000003.12:g.64726228C>T
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

4607103

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605421.G.1Lebanon1961BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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