NM_001363894.1:c.46-13587A>G

HGVS Expressions

  • NG_012969.1:g.97591A>G
  • NM_001363894.1:c.46-13587A>G
  • NP_001350823.1:p.?
  • NC_000016.10:g.53796553A>G
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

9930506

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610966.G.5.2United Arab Emirates700.43Uncertain SignificanceSaber-Ayad et al. 2019 Group of 35/169 subjects with rs9930506 ...
610966.G.6.4United Arab Emirates1220.46Saber-Ayad et al. 2019 Study with 259 Emiratis.
610966.G.6.5United Arab Emirates1120.46Saber-Ayad et al. 2019 Study with 259 Emiratis.
610966.G.7.1United Arab Emirates1580.43Naja et al. 2021 Healthy subjects.
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