NM_001379610.1:c.101A>G

HGVS Expressions

  • NG_008356.2:g.16117A>G
  • NM_001379610.1:c.101A>G
  • NP_003113.2:p.Asn34Ser
  • NC_000005.10:g.147828115T>C
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Clinvar Clinical Significance

Association, Likely Benign, Likely Pathogenic, Pathogenic, Risk factor, Uncertain Significance

CTGA Clinical Significance

Risk factor

Variant Type

Substitution

Clinvar

13760

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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