List of variants in gene combination AMN, LOC130056554 reported as pathogenic for hematologic disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_030943.4(AMN):c.1006+11_1008del	rs1566829097
NM_030943.4(AMN):c.1006+34_1007-31del	rs386834161
NM_030943.4(AMN):c.1041_1042delinsCTC (p.Glu348fs)	rs2139312594
NM_030943.4(AMN):c.1114dup (p.Ala372fs)
NM_030943.4(AMN):c.968_975del (p.Arg323fs)

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