List of variants in gene DNM1L reported by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.*1120A>G	rs143037211	0.01488
NM_012062.5(DNM1L):c.2102_2103dup	rs140265365	0.01081
NM_012062.5(DNM1L):c.*1538del	rs376738847	0.00152
NM_012062.5(DNM1L):c.275_278dup	rs781178788	0.00044
NM_012062.5(DNM1L):c.*1526T>C	rs758547863	0.00008
NM_012062.5(DNM1L):c.1597-3_1597-2dup	rs768493019	0.00005
NM_012062.5(DNM1L):c.1471_1475dup	rs1555133474	0.00001
NM_012062.5(DNM1L):c.*1315dup	rs370524523
NM_012062.5(DNM1L):c.*1338C>T	rs190574893
NM_012062.5(DNM1L):c.21_22delinsCT	rs34421401
NM_012062.5(DNM1L):c.*2206dup	rs886049302
NM_012062.5(DNM1L):c.335_338dup	rs568956138

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