List of variants in gene DNM2 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.1077C>T (p.Gly359=)	rs112238216	0.02416
NM_001005361.3(DNM2):c.2484G>A (p.Pro828=)	rs114682382	0.01064
NM_001005361.3(DNM2):c.235+12C>A	rs147026993	0.00953
NM_001005361.3(DNM2):c.1782-11C>T	rs78580529	0.00921
NM_001005361.3(DNM2):c.235+6A>G	rs113192269	0.00748
NM_001005361.3(DNM2):c.2543+7C>G	rs201979143	0.00364
NM_001005361.3(DNM2):c.236-8C>G	rs143084059	0.00361
NM_001005361.3(DNM2):c.519T>C (p.Ala173=)	rs77702567	0.00359
NM_001005361.3(DNM2):c.1545+14C>G	rs114713494	0.00350
NM_001005361.3(DNM2):c.1902C>T (p.Asn634=)	rs2229919	0.00149
NM_001005361.3(DNM2):c.1218C>T (p.Asp406=)	rs147668465	0.00116
NM_001005361.3(DNM2):c.1782-5C>T	rs200103145	0.00113

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