ClinVar Miner

List of variants studied for anemia, congenital dyserythropoietic, type 1a by Centogene AG - the Rare Disease Company

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_138477.4(CDAN1):c.156C>G (p.Phe52Leu) rs80338694 0.00009
NM_138477.4(CDAN1):c.2174G>A (p.Arg725Gln) rs962870388 0.00001

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