List of variants in gene ALS2 reported as likely benign for ALS2-Related Disorders

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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_020919.4(ALS2):c.*379T>A	rs144613080	0.00995
NM_020919.4(ALS2):c.*163A>G	rs3219172	0.00975
NM_020919.4(ALS2):c.*942A>G	rs41309066	0.00903
NM_020919.4(ALS2):c.4581-7A>G	rs114458388	0.00827
NM_020919.4(ALS2):c.3625-16_3625-15del	rs370628135	0.00777
NM_020919.4(ALS2):c.4119A>G (p.Ile1373Met)	rs61757691	0.00269
NM_020919.4(ALS2):c.3309T>C (p.His1103=)	rs201920363	0.00184
NM_020919.4(ALS2):c.3905G>A (p.Arg1302His)	rs199577696	0.00105
NM_020919.4(ALS2):c.1115C>G (p.Pro372Arg)	rs190369242	0.00100
NM_020919.4(ALS2):c.3462G>A (p.Gln1154=)	rs556027390	0.00013

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