List of variants in gene HSPB1 reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001540.5(HSPB1):c.178C>T (p.Pro60Ser)	rs61751217	0.00153
NM_001540.5(HSPB1):c.-19C>T	rs199602956	0.00149
NM_001540.5(HSPB1):c.24C>T (p.Phe8=)	rs201769668	0.00024
NM_001540.5(HSPB1):c.501C>T (p.Ala167=)	rs529095936	0.00007
NM_001540.5(HSPB1):c.210G>A (p.Ala70=)	rs749963653	0.00006
NM_001540.5(HSPB1):c.365-96C>G
NM_001540.5(HSPB1):c.411C>T (p.Cys137=)	rs1803060234

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