List of variants in gene IARS2 studied for bone development disease

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_018060.4(IARS2):c.2122G>A (p.Glu708Lys)	rs143722284	0.00089
NM_018060.4(IARS2):c.1016C>T (p.Ser339Phe)	rs139437119	0.00061
NM_018060.4(IARS2):c.2620G>A (p.Gly874Arg)	rs151241066	0.00004
NM_018060.4(IARS2):c.601C>T (p.Arg201Cys)	rs768101579	0.00001
NM_018060.4(IARS2):c.1255G>A (p.Asp419Asn)	rs745601033
NM_018060.4(IARS2):c.1328-5dup	rs199649609
NM_018060.4(IARS2):c.1504A>C (p.Ile502Leu)	rs747014267
NM_018060.4(IARS2):c.1821G>A (p.Trp607Ter)	rs373436822
NM_018060.4(IARS2):c.2282A>G (p.His761Arg)	rs1571863769
NM_018060.4(IARS2):c.2450G>A (p.Arg817His)	rs146618526
NM_018060.4(IARS2):c.268-8del	rs376359534
NM_018060.4(IARS2):c.2725C>T (p.Pro909Ser)	rs1571865562
NM_018060.4(IARS2):c.2726C>T (p.Pro909Leu)	rs587783070
NM_018060.4(IARS2):c.680T>C (p.Phe227Ser)	rs1571845061
NM_018060.4(IARS2):c.991G>A (p.Val331Ile)

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