List of variants reported as benign for hematologic disorder by Dunham Lab, University of Washington

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Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.1365-13C>T	rs2071429	0.63462
NM_001042351.2(G6PD):c.-111A>G	rs111827785	0.14433
NM_001360016.2(G6PD):c.121-135A>G	rs762515	0.10367
NM_001360016.2(G6PD):c.864+163C>T	rs5986990	0.09646
NM_001360016.2(G6PD):c.1116G>A (p.Gln372=)	rs2230036	0.03373
NM_001360016.2(G6PD):c.337G>A (p.Asp113Asn)	rs5030870	0.00005
NM_001360016.2(G6PD):c.690C>T (p.Ile230=)	rs781917123	0.00005
NM_001360016.2(G6PD):c.*304T>C
NM_001360016.2(G6PD):c.107T>C (p.Ile36Thr)
NM_001360016.2(G6PD):c.120+199dup	rs781893284
NM_001360016.2(G6PD):c.120+2955A>G
NM_001360016.2(G6PD):c.120+3126T>C
NM_001360016.2(G6PD):c.121-1792T>C
NM_001360016.2(G6PD):c.121-1813del
NM_001360016.2(G6PD):c.121-2107T>C
NM_001360016.2(G6PD):c.121-2679C>G
NM_001360016.2(G6PD):c.121-4460del
NM_001360016.2(G6PD):c.1311= (p.Tyr437=)	rs2230037
NM_001360016.2(G6PD):c.1422G>A (p.Leu474=)
NM_001360016.2(G6PD):c.445G>A (p.Ala149Thr)
NM_001360016.2(G6PD):c.[1116G>A;1311=]

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