List of variants in gene DNM1L reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.252G>A (p.Gly84=)	rs2272238	0.15635
NM_012062.5(DNM1L):c.120A>C (p.Ser40=)	rs10844308	0.14357
NM_012062.5(DNM1L):c.918A>G (p.Thr306=)	rs10844318	0.14349
NM_012062.5(DNM1L):c.1968C>T (p.Leu656=)	rs148634653	0.01775
NM_012062.5(DNM1L):c.741-19G>A	rs79520527	0.00897
NM_012062.5(DNM1L):c.1470A>G (p.Glu490=)	rs79393011	0.00828

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