List of variants reported as likely pathogenic for anemia, nonspherocytic hemolytic by Revvity Omics, Revvity

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.968T>C (p.Leu323Pro)	rs76723693	0.00154
NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe)	rs137852342	0.00003
NM_000402.4(G6PD):c.298T>C (p.Tyr100His)	rs137852349	0.00002
NM_001360016.2(G6PD):c.209A>G (p.Tyr70Cys)	rs782090947	0.00002
NM_001360016.2(G6PD):c.406C>T (p.Arg136Cys)	rs979416826	0.00002
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr)	rs76645461	0.00001
G6PD NARA	rs587776730
NM_000402.4(G6PD):c.1246A>G (p.Lys416Glu)	rs137852320
NM_000402.4(G6PD):c.1318G>T (p.Gly440Cys)	rs137852323
NM_000402.4(G6PD):c.1406G>C (p.Arg469Pro)	rs137852337
NM_000402.4(G6PD):c.482G>T (p.Gly161Val)	rs137852341
NM_001360016.2(G6PD):c.1318C>T (p.Leu440Phe)	rs1557229599
NM_001360016.2(G6PD):c.1358T>A (p.Val453Glu)
NM_001360016.2(G6PD):c.383T>G (p.Leu128Arg)	rs78365220
NM_001360016.2(G6PD):c.835A>T (p.Thr279Ser)	rs2148329890

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