List of variants in gene NARS2 reported by OMIM

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_024678.6(NARS2):c.167A>G (p.Gln56Arg)	rs201751992	0.00005
NM_024678.6(NARS2):c.641C>T (p.Pro214Leu)	rs730882155	0.00003
NM_024678.6(NARS2):c.151C>T (p.Arg51Cys)	rs367584549	0.00002
NM_024678.6(NARS2):c.500A>G (p.His167Arg)	rs750594551	0.00001
NM_024678.6(NARS2):c.631T>A (p.Phe211Ile)	rs755122704	0.00001
NM_024678.6(NARS2):c.1184T>G (p.Leu395Arg)	rs763770414
NM_024678.6(NARS2):c.594+1G>A	rs1035101172
NM_024678.6(NARS2):c.637G>T (p.Val213Phe)	rs756725793
NM_024678.6(NARS2):c.707T>G (p.Phe236Cys)	rs1565235204
NM_024678.6(NARS2):c.822G>C (p.Gln274His)	rs730882154
NM_024678.6(NARS2):c.969T>A (p.Tyr323Ter)	rs565224393

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