List of variants reported as pathogenic for anemia by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.1478G>A (p.Arg493His)	rs72554664	0.00012
NM_206965.2(FTCD):c.990dup (p.Pro331fs)	rs398124234

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