NM_170735.6:c.196G>A

HGVS Expressions

  • NG_011794.1:g.68690G>A
  • NM_170735.6:c.196G>A
  • NP_733931.1:p.Val66Met
  • NC_000011.10:g.27658369C>T
Back to search Result
Clinvar Clinical Significance

Benign, Risk factor

Variant Type

Substitution

dbSNP

6265

Clinvar

17697

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601665.G.3.1United Arab Emirates820.131ObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates1000.129El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
605552.G.3.1United Arab Emirates0.123Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.183Osman et al. 2020b 104 control subjects
© CAGS 2024. All rights reserved.