NM_198353.2:c.961+94716G>A

HGVS Expressions

  • NM_198353.2:c.961+94716G>A
  • NP_938167.1:p.?
  • NC_000004.12:g.44352847C>T
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Variant Type

Substitution

dbSNP

7675224

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.35.1United Arab EmiratesNA0.81Al Safar et al. 2013 Discovery GWAS group comprising 178 indi...
125853.G.35.2ArabNANAAl Safar et al. 2013 Replication sample group comprising 315 ...
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