List of variants in gene DNAJB6 reported as likely benign for Myofibrillar Myopathy, Dominant

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_058246.4(DNAJB6):c.*639A>G	rs76450641	0.00706
NM_058246.4(DNAJB6):c.*776C>T	rs115297289	0.00683
NM_058246.4(DNAJB6):c.-86G>A	rs562984002	0.00659
NM_058246.4(DNAJB6):c.*72C>T	rs116630040	0.00519
NM_058246.4(DNAJB6):c.*88G>A	rs139193261	0.00398
NM_058246.4(DNAJB6):c.*489T>C	rs187704048	0.00309
NM_058246.4(DNAJB6):c.279C>T (p.Phe93=)	rs149278319	0.00191
NM_058246.4(DNAJB6):c.-43G>T	rs566594165	0.00060
NM_058246.4(DNAJB6):c.*902C>T	rs547235102	0.00056
NM_058246.4(DNAJB6):c.692-13G>T	rs192981897	0.00038

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