List of variants reported as uncertain significance for amyotrophic lateral sclerosis type 1 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000454.5(SOD1):c.*153T>G	rs188029963	0.00203
NM_000454.5(SOD1):c.420C>T (p.Asn140=)	rs1804449	0.00005
NM_000454.4(SOD1):c.-84C>G	rs573544165	0.00003
NM_000454.5(SOD1):c.457G>A (p.Ala153Thr)	rs747094021	0.00002
NM_000454.5(SOD1):c.66G>A (p.Glu22=)	rs756458346	0.00002
NM_000454.5(SOD1):c.328G>T (p.Asp110Tyr)	rs567432143	0.00001
NM_000454.4(SOD1):c.-87G>A	rs139202139
NM_000454.4(SOD1):c.-87G>C	rs139202139
NM_000454.4(SOD1):c.-91C>G	rs568985632
NM_000454.5(SOD1):c.*198G>A	rs2049623017
NM_000454.5(SOD1):c.-55C>G	rs16988395
NM_000454.5(SOD1):c.-55C>T	rs16988395
NM_000454.5(SOD1):c.-56T>A	rs535066119
NM_000454.5(SOD1):c.331C>T (p.His111Tyr)	rs2049603707
NM_000454.5(SOD1):c.75A>G (p.Glu25=)	rs2049569274

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