List of variants reported as uncertain significance for anemia by SIB Swiss Institute of Bioinformatics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001321759.2(CDIN1):c.707A>G (p.Tyr236Cys)	rs768744226	0.00002
NM_001321759.2(CDIN1):c.59C>G (p.Pro20Arg)	rs1595696464

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