List of variants in gene IARS2 reported as likely benign for not specified

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_018060.4(IARS2):c.2897-15T>C	rs191806652	0.00228
NM_018060.4(IARS2):c.390+10A>G	rs201829262	0.00096
NM_018060.4(IARS2):c.2122G>A (p.Glu708Lys)	rs143722284	0.00089
NM_018060.4(IARS2):c.2307+14A>G	rs201438337	0.00029
NM_018060.4(IARS2):c.990C>T (p.Tyr330=)	rs377623873	0.00020
NM_018060.4(IARS2):c.1328-18G>T	rs551635063	0.00012
NM_018060.4(IARS2):c.636C>T (p.Tyr212=)	rs141996928	0.00007
NM_018060.4(IARS2):c.2316A>G (p.Glu772=)	rs377178843	0.00004
NM_018060.4(IARS2):c.1770T>C (p.Tyr590=)	rs768336894	0.00003
NM_018060.4(IARS2):c.453C>T (p.Pro151=)	rs756654341	0.00003
NM_018060.4(IARS2):c.1554A>T (p.Pro518=)	rs775197017	0.00001
NM_018060.4(IARS2):c.267+8C>A	rs755614129	0.00001
NM_018060.4(IARS2):c.1020T>G (p.Val340=)	rs1553268086
NM_018060.4(IARS2):c.1947-20del	rs774380565
NM_018060.4(IARS2):c.2897-5dup	rs781485617
NM_018060.4(IARS2):c.300A>G (p.Gln100=)	rs1553267547
NM_018060.4(IARS2):c.492A>G (p.Val164=)	rs1057521649
NM_018060.4(IARS2):c.699+17dup	rs571001903

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