List of variants in gene GSR reported as likely benign for 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.1069A>G (p.Ile357Val)	rs75673983	0.00632
NM_000637.5(GSR):c.1500G>A (p.Thr500=)	rs368833049	0.00014
NM_000637.5(GSR):c.531G>T (p.Thr177=)	rs147119692

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