NM_000197.1:c.823-67_823-59del

HGVS Expressions

  • NG_008157.1:g.71516_71524del
  • NM_000197.1:c.823-67_823-59del
  • NP_000188.1:p.?
  • NC_000009.12:g.96235634_96235642del
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Clinvar Clinical Significance

Benign

Variant Type

Indel

dbSNP

3831056

Clinvar

1220642

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.407Almheiri et al. 2019 500 healthy Emiratis (254 females)
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