List of variants in gene combination OR10Z1, SPTA1 reported as likely 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.*68C>G	rs186892978	0.00406
NM_003126.4(SPTA1):c.*387T>C	rs549664412	0.00146

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