NM_003995.3:c.3079-49A>G

HGVS Expressions

  • NG_009249.1:g.21923A>G
  • NM_003995.3:c.3079-49A>G
  • NP_003986.2:p.?
  • NC_000009.12:g.35809331A>G
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2281645

Clinvar

1250991

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.26.2United Arab EmiratesNA0.193AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Male subjects from a group of 897 T2DM p...
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