Variants in gene HSPB1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_001540.5(HSPB1):c.36G>T (p.Arg12=)	rs145369859	0.00486
NM_001540.5(HSPB1):c.9G>A (p.Glu3=)	rs77586767	0.00336
NM_001540.5(HSPB1):c.573T>C (p.Leu191=)	rs34771861	0.00170
NM_001540.5(HSPB1):c.178C>T (p.Pro60Ser)	rs61751217	0.00153
NM_001540.5(HSPB1):c.240A>G (p.Gln80=)	rs377246178	0.00056
NM_001540.5(HSPB1):c.438C>T (p.Pro146=)	rs7805625	0.00049
NM_001540.5(HSPB1):c.501C>T (p.Ala167=)	rs529095936	0.00007
NM_001540.5(HSPB1):c.318G>C (p.Pro106=)	rs750349055

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