NR_038309.1:n.332+12925C>T

HGVS Expressions

  • NR_038309.1:n.332+12925C>T
  • NC_000011.10:g.42225168G>A
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

7480010

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
LINC02740.G.1Lebanon1606BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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