NM_001379610.1:c.56-37T>C

HGVS Expressions

  • NG_008356.2:g.14565T>C
  • NM_001379610.1:c.56-37T>C
  • NC_000005.10:g.147829667A>G
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Clinvar Clinical Significance

Benign, Risk factor

CTGA Clinical Significance

Risk factor

Variant Type

Substitution

Clinvar

239507

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
167800.1United Arab Emirates1Risk factorPancreatitis, HereditaryAbass et al. 2022
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