NG_008731.1:g.1270G>A

HGVS Expressions

  • NG_008731.1:g.1270G>A
  • NG_008731.1:g.1270G>A

Associated Genes

Vitamin D Receptor
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Genomic Location

chr12:47908762

CTGA Clinical Significance

Association

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601769.G.2.2Lebanon1190.17AssociationHajj et al. 2016 Group of healthy individuals including 1...
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