NC_000004.12:g.81233556T>C

HGVS Expressions

  • NC_000004.12:g.81233556T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

1712374

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.26.3United Arab EmiratesNA0.278AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Female subjects from a group of 897 T2DM...
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