NM_001114974.2:c.1259+2577G>A

HGVS Expressions

  • NM_001114974.2:c.1259+2577G>A
  • NP_001108446.1:p.?
  • NC_000017.11:g.4599900G>A
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CTGA Clinical Significance

Protective

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
180300.G.1Arab0.14ProtectiveRheumatoid ArthritisSaxena et al. 2017 511 cases compared to 352 controls; all ...
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