List of variants in gene AMN reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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.1170-37C>G	rs148815688	0.29891
NM_030943.4(AMN):c.363G>A (p.Gly121=)	rs141455061	0.00632
NM_030943.4(AMN):c.829A>G (p.Thr277Ala)	rs146499374	0.00428
NM_030943.4(AMN):c.1343_1348dup (p.Gly448_Ala449dup)	rs36040113
NM_030943.4(AMN):c.514-34G>C	rs144077391

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