NG_013364.1:g.3473=

HGVS Expressions

  • NG_013364.1:g.3473=
  • NC_000019.10:g.41355454=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

4803457

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.41.7United Arab EmiratesNA0.429AssociationType 2 Diabetes MellitusElHajj Chehadeh et al. 2021 Study with 158 T2DM patients (T2DM assoc...
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