List of variants in gene HSPB1 reported as likely benign by GeneDx

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001540.5(HSPB1):c.364+34A>C	rs34957294	0.01483
NC_000007.14:g.76304401C>T	rs147012280	0.01327
NM_001540.5(HSPB1):c.428+44T>G	rs568301666	0.01291
NM_001540.5(HSPB1):c.365-257C>T	rs36073761	0.01042
NM_001540.5(HSPB1):c.365-60C>T	rs11769502	0.00986
NC_000007.14:g.76304449G>C	rs34428939	0.00932
NM_001540.5(HSPB1):c.365-258G>C	rs188825703	0.00801
NC_000007.14:g.76304433C>T	rs117510558	0.00798
NM_001540.5(HSPB1):c.*86C>A	rs113923827	0.00562
NM_001540.5(HSPB1):c.36G>T (p.Arg12=)	rs145369859	0.00447
NC_000007.14:g.76302359C>T	rs6963310	0.00442
NM_001540.5(HSPB1):c.365-189A>G	rs112258813	0.00441
NM_001540.4(HSPB1):c.-56C>T	rs35759978	0.00315
NM_001540.5(HSPB1):c.*22C>T	rs557532119	0.00300
NM_001540.5(HSPB1):c.573T>C (p.Leu191=)	rs34771861	0.00170
NM_001540.5(HSPB1):c.-19C>T	rs199602956	0.00145
NM_001540.5(HSPB1):c.240A>G (p.Gln80=)	rs377246178	0.00050
NM_001540.5(HSPB1):c.438C>T (p.Pro146=)	rs7805625	0.00042
NM_001540.5(HSPB1):c.24C>T (p.Phe8=)	rs201769668	0.00022
NM_001540.5(HSPB1):c.365-7C>G	rs201897299	0.00011
NM_001540.5(HSPB1):c.501C>T (p.Ala167=)	rs529095936	0.00007
NM_001540.5(HSPB1):c.210G>A (p.Ala70=)	rs749963653	0.00005
NM_001540.5(HSPB1):c.-15G>A	rs756260929	0.00004
NM_001540.5(HSPB1):c.84C>T (p.Leu28=)	rs778672047	0.00001
NC_000007.14:g.76302412G>C	rs117458699
NM_001540.5(HSPB1):c.318G>C (p.Pro106=)	rs750349055
NM_001540.5(HSPB1):c.364+317dup	rs546337268
NM_001540.5(HSPB1):c.365-5C>T	rs368936457
NM_001540.5(HSPB1):c.610G>A (p.Ala204Thr)	rs367857772

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