List of variants in gene G6PD reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.466A>G (p.Asn156Asp)	rs1050829	0.08672
NM_001360016.2(G6PD):c.645-17C>T	rs5986875	0.00915
NM_001360016.2(G6PD):c.1048G>C (p.Asp350His)	rs34193178	0.00110
NM_001360016.2(G6PD):c.1457+31C>G	rs373239864	0.00050
NM_001360016.2(G6PD):c.864+17A>T	rs377041776	0.00019
NM_001360016.2(G6PD):c.519C>T (p.Phe173=)	rs200111236	0.00010
NM_001360016.2(G6PD):c.957C>T (p.Thr319=)	rs199702562	0.00010
NM_001360016.2(G6PD):c.1405C>T (p.Leu469=)	rs369482861	0.00008
NM_001360016.2(G6PD):c.771-8G>A	rs368790003	0.00004
NM_001360016.2(G6PD):c.1288-14TC[2]	rs199586268
NM_001360016.2(G6PD):c.318C>T (p.Ser106=)	rs2148331419
NM_001360016.2(G6PD):c.864+8dup	rs782714017

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