List of variants in gene AARS1 reported as likely benign for epilepsy

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001605.3(AARS1):c.2900A>T (p.Lys967Met)	rs35744709	0.00971
NM_001605.3(AARS1):c.1404C>T (p.Tyr468=)	rs117598688	0.00646
NM_001605.3(AARS1):c.1672-4T>A	rs187509039	0.00236
NM_001605.3(AARS1):c.700C>T (p.Pro234Ser)	rs141840552	0.00137
NM_001605.3(AARS1):c.1044G>C (p.Thr348=)	rs181264712	0.00067
NM_001605.3(AARS1):c.1007A>G (p.His336Arg)	rs1025002934	0.00001
NM_001605.3(AARS1):c.1664G>T (p.Ser555Ile)	rs144982168	0.00001
NM_001605.3(AARS1):c.-21-11dup	rs756492963

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