List of variants in gene HSPB1 reported as likely benign 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_001540.5(HSPB1):c.9G>A (p.Glu3=)	rs77586767	0.00336
NM_001540.5(HSPB1):c.498G>A (p.Glu166=)	rs148357753	0.00002

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