List of variants in gene combination CDAN1, LOC130056931 reported as likely benign for Anemia, congenital dyserythropoietic, type 1a

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.309G>T (p.Pro103=)	rs575562332	0.00350
NM_138477.4(CDAN1):c.237G>C (p.Ser79=)	rs180857061	0.00344
NM_138477.4(CDAN1):c.375G>A (p.Pro125=)

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