NM_032784.4:c.634+134=

HGVS Expressions

  • NM_032784.4:c.634+134=
  • NP_116173.2:p.?
  • NC_000006.12:g.127155572=

Associated Genes

R-Spondin 3
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Variant Type

Reference Allele

dbSNP

2489629

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.1United Arab Emirates0.449Osman et al. 2018 450 patients with T2DM
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