List of variants in gene YARS2 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_001040436.3(YARS2):c.1275-323A>G	rs3789979	0.40907
NM_001040436.2(YARS2):c.-153G>C	rs3827883	0.14359
NM_001040436.3(YARS2):c.291C>T (p.Gly97=)	rs11539444	0.14354
NM_001040436.3(YARS2):c.572G>T (p.Gly191Val)	rs11539445	0.14334
NM_001040436.3(YARS2):c.1104-107A>C	rs10844339	0.12522
NM_001040436.3(YARS2):c.1274+187_1274+189dup	rs369800082	0.04726
NM_001040436.3(YARS2):c.1274+159G>A	rs61926203	0.02962
NM_001040436.3(YARS2):c.1026G>A (p.Arg342=)	rs35339227	0.02168
NM_001040436.3(YARS2):c.948-281G>A	rs139971581	0.02137
NM_001040436.3(YARS2):c.1104-211G>A	rs143432850	0.01984
NM_001040436.3(YARS2):c.1103+18T>C	rs190343859	0.00622
NM_001040436.3(YARS2):c.342C>T (p.Gly114=)	rs115606831	0.00371
NM_001040436.3(YARS2):c.1275-2dup	rs565781501	0.00357
NM_001040436.3(YARS2):c.456G>A (p.Ala152=)	rs201940521	0.00157
NM_001040436.3(YARS2):c.104C>A (p.Ala35Asp)	rs149447502	0.00151
NM_001040436.3(YARS2):c.870T>C (p.Val290=)	rs142067801	0.00041
NM_001040436.3(YARS2):c.1104-16dup	rs761612441
NM_001040436.3(YARS2):c.930G>A (p.Pro310=)	rs147551647
NM_001040436.3(YARS2):c.948-211dup	rs57698169

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