NM_001025366.2:c.855+175C>T

HGVS Expressions

  • NG_008732.1:g.12625C>T
  • NM_001025366.2:c.855+175C>T
  • NP_001020537.2:p.?
  • NC_000006.12:g.43777840C>T
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

3024998

Clinvar

1285895

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.41.1United Arab EmiratesNA0.36AssociationType 2 Diabetes MellitusElHajj Chehadeh et al. 2021 Study with 158 T2DM patients; 35 patient...
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