List of variants in gene HSPB1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001540.5(HSPB1):c.287del (p.Arg96fs)	rs1803029816
NM_001540.5(HSPB1):c.407G>A (p.Arg136Gln)	rs863225022
NM_001540.5(HSPB1):c.438dup (p.Gly147fs)	rs747325717
NM_001540.5(HSPB1):c.504del (p.Met169fs)

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