NM_000376.3:c.1056T>C

HGVS Expressions

  • NG_008731.1:g.65058T>C
  • NM_000376.3:c.1056T>C
  • NP_000367.1:p.Ile352=
  • NC_000012.12:g.47844974A>G

Associated Genes

Vitamin D Receptor
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Clinical Significance

Benign,Likely Benign

Variant Type

Substitution

dbSNP

731236

Clinvar

308877

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
176807.G.1.1Lebanon56BenignProstate CancerEl Ezzi et al. 2017 69 patients with confirmed prostate cancer
176807.G.1.2Lebanon52BenignEl Ezzi et al. 2017 69 Lebanese control subjects
600082.G.1.1LebanonBenignEl Ezzi et al. 2014 68 patients with BPH. VDR SNPs (c.2T>G) ...
600082.G.1.2LebanonEl Ezzi et al. 2014 79 Lebanese controls
601769.G.1.1United Arab Emirates229BenignOsman et al. 2015 Group of healthy individuals including 1...
601769.G.2.4Lebanon290AssociationHajj et al. 2016 Group of healthy individuals including 5...
601769.G.3.3Lebanon48BenignArabi et al. 2009 VDR polymorphisms (using Bsm1 and Taq1 e...
601769.G.3.4Lebanon89BenignArabi et al. 2009 VDR polymorphisms (using Bsm1 and Taq1 e...
601769.G.4.5Lebanon170BenignArabi et al. 2010 Study on healthy individuals. Heterozygo...
601769.G.4.6Lebanon94BenignArabi et al. 2010 Study on healthy individuals. Heterozygo...
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