NC_000011.10:g.86157598=

HGVS Expressions

  • NC_000011.10:g.86157598=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

3851179

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
104300.G.2.1Lebanon370.31AssociationAlzheimer DiseaseMasri et al, 2019 Study with 59 Alzheimer disease patients
104300.G.2.2Lebanon390.39Masri et al, 2019 Group consisting of 50 control subjects
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