List of variants in gene SETX reported as uncertain significance for spinal muscular atrophy

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_015046.7(SETX):c.2672T>C (p.Val891Ala)	rs148181729	0.00470
NM_015046.7(SETX):c.7711C>T (p.Pro2571Ser)	rs1554801479

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