List of variants reported as benign for anemia by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.466A>G (p.Asn156Asp)	rs1050829	0.08672
NM_000324.3(RHAG):c.808G>A (p.Val270Ile)	rs16879498	0.04007
NM_000037.4(ANK1):c.5097-34C>T	rs185434561	0.00261
NM_000298.6(PKLR):c.375+10G>T	rs8177971
NM_001022.4(RPS19):c.356+18G>C	rs61762294

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