List of variants in gene combination AMN, LOC130056553 reported as 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_030943.4(AMN):c.208-10T>C	rs115851517	0.00345
NM_030943.4(AMN):c.208-16C>T	rs202004969	0.00214

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