List of variants in gene combination ANG, EGILA, RNASE4 reported as likely pathogenic for amyotrophic lateral sclerosis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001097577.3(ANG):c.407C>T (p.Pro136Leu)	rs121909543	0.00002
NM_001097577.3(ANG):c.155G>A (p.Ser52Asn)	rs121909542	0.00001

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