List of variants in gene GSR reported as benign for familial hemolytic anemia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000637.5(GSR):c.696-10C>T	rs8190996	0.41377
NM_000637.5(GSR):c.457C>T (p.Arg153Cys)	rs8190955	0.02941
NM_000637.5(GSR):c.334-4dup	rs112134304	0.02050

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