NM_016729.3:c.1A>G

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  2. NM_016729.3:c.1A>G

HGVS Expressions

  • NG_015863.1:g.7617A>G
  • NM_016729.3:c.1A>G
  • NP_057941.1:p.Met1?
  • NC_000011.10:g.72192174A>G

Associated Genes

Folate Receptor, Alpha
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Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

dbSNP

1057524829

Clinvar

393190

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
136430.1Qatar10.009PathogenicDevadoss Gandhi et al. 2024 1 individual from a study of 14,060 Qata...
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Contributors

  • Sayeeda Hana: 13.12.2024

Edit History

  • Sayeeda Hana: 13.12.2024
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.