List of variants in gene RARS1 reported as likely pathogenic 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002887.4(RARS1):c.1367C>T (p.Ser456Leu)	rs139644798	0.00044
NM_002887.4(RARS1):c.1534C>T (p.Arg512Trp)	rs757249400	0.00002
NM_002887.4(RARS1):c.1535G>A (p.Arg512Gln)	rs369398935	0.00002
NM_002887.4(RARS1):c.1414C>T (p.Arg472Ter)	rs180760483	0.00001
NM_002887.4(RARS1):c.1452+1G>A	rs1358682351	0.00001
NM_002887.4(RARS1):c.1283G>A (p.Trp428Ter)
NM_002887.4(RARS1):c.1579dup (p.Arg527fs)
NM_002887.4(RARS1):c.175C>T (p.Arg59Ter)	rs749027104
NM_002887.4(RARS1):c.180+2T>C	rs778874286
NM_002887.4(RARS1):c.448_456del (p.Cys150_Glu152del)	rs768923402

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