List of variants in gene combination DNM1L, YARS2 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_001040436.3(YARS2):c.*209G>C	rs10844337	0.15609
NM_012062.5(DNM1L):c.*271C>G	rs1020670	0.15598
NM_012062.5(DNM1L):c.*1213G>T	rs11052213	0.15596
NM_012062.5(DNM1L):c.*744A>T	rs1971911	0.15585
NM_012062.5(DNM1L):c.*21G>C	rs1059422	0.15548
NM_012062.5(DNM1L):c.*22A>T	rs3200103	0.15544
NM_001040436.3(YARS2):c.*643G>A	rs11052214	0.14502
NM_012062.5(DNM1L):c.*1242G>A	rs10844336	0.14342
NM_012062.5(DNM1L):c.*600C>T	rs3600	0.08008
NM_012062.5(DNM1L):c.*1415T>C	rs114366772	0.01556
NM_001040436.3(YARS2):c.*191T>C	rs144235100	0.01314
NM_012062.5(DNM1L):c.*1156G>C	rs148183516	0.01245
NM_001040436.3(YARS2):c.*162A>G	rs11052215	0.01096
NM_001040436.3(YARS2):c.1356A>G (p.Gln452=)	rs148729348	0.00975
NM_001040436.3(YARS2):c.126_127del	rs141873255	0.00137
NM_001040436.3(YARS2):c.*360A>G	rs567955032	0.00069
NM_001040436.3(YARS2):c.*142T>C	rs190589666	0.00010
NM_001040436.3(YARS2):c.*230A>G	rs371690622	0.00001
NM_001040436.3(YARS2):c.*406C>T	rs145618550
NM_001040436.3(YARS2):c.*62G>A	rs527443669
NM_012062.5(DNM1L):c.*393A>C	rs77298476

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