NM_018268.4:c.697+515_697+518del

HGVS Expressions

  • NM_018268.4:c.697+515_697+518del
  • NP_060738.2:p.?
  • NC_000005.10:g.77449249_77449252del
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Variant Type

Microsatellite

dbSNP

1610937

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.593Almheiri et al. 2019 500 healthy Emiratis (254 females)
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