ClinVar Miner

List of variants in gene combination CDAN1, LOC130056932 reported as likely benign for anemia, congenital dyserythropoietic, type 1a

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_138477.4(CDAN1):c.114G>A (p.Ala38=) rs560030704 0.00005

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