ClinVar Miner

List of variants in gene RARS2 reported by Neuberg Centre For Genomic Medicine, NCGM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020320.5(RARS2):c.25A>G (p.Ile9Val)	rs748335175	0.00002
NM_020320.5(RARS2):c.1152G>T (p.Lys384Asn)	rs1582278290
NM_020320.5(RARS2):c.284_285del (p.Glu95fs)	rs767056243
NM_020320.5(RARS2):c.602A>G (p.His201Arg)

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