List of variants in gene combination ANG, EGILA, RNASE4 reported as uncertain significance for amyotrophic lateral sclerosis type 9

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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_001097577.3(ANG):c.122A>T (p.Lys41Ile)	rs121909536	0.00091
NM_001097577.3(ANG):c.208A>G (p.Ile70Val)	rs121909541	0.00073
NM_001097577.3(ANG):c.3G>A (p.Met1Ile)	rs201068740	0.00020
NM_001097577.3(ANG):c.62C>T (p.Pro21Leu)	rs773237991	0.00002
NM_001097577.3(ANG):c.38T>C (p.Val13Ala)	rs200240901	0.00001
NM_001097577.3(ANG):c.433C>T (p.Arg145Cys)	rs565444731	0.00001
NM_001097577.3(ANG):c.*81A>C	rs550007170
NM_001097577.3(ANG):c.-18-4G>A	rs373669465
NM_001097577.3(ANG):c.224G>A (p.Arg75His)	rs146485834
NM_001097577.3(ANG):c.368G>A (p.Gly123Glu)	rs535311762

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