NG_002432.1:g.31279G>C

HGVS Expressions

  • NG_002432.1:g.31279G>C
  • NC_000006.12:g.32484011G>C
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CTGA Clinical Significance

Protective

Variant Type

Substitution

dbSNP

9269234

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
180300.G.1Arab0.35ProtectiveRheumatoid ArthritisSaxena et al. 2017 511 cases compared to 352 controls; all ...
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