List of variants in gene DNAJC19 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_145261.4(DNAJC19):c.130-292T>C	rs1805637	0.02945
NM_145261.4(DNAJC19):c.4-128_4-127insG	rs766807321	0.01035
NM_145261.4(DNAJC19):c.281-160A>T	rs139914001	0.00525
NM_145261.4(DNAJC19):c.280+129G>A	rs115056126	0.00503
NM_145261.4(DNAJC19):c.300A>G (p.Ala100=)	rs373886730	0.00044
NM_145261.4(DNAJC19):c.3+16C>T	rs367841424	0.00013
NM_145261.4(DNAJC19):c.129+15A>C	rs201697391	0.00010
NM_145261.4(DNAJC19):c.90G>A (p.Glu30=)	rs367996239	0.00002
NM_145261.4(DNAJC19):c.130-38_130-34del	rs145145539
NM_145261.4(DNAJC19):c.209+95C>G	rs192120432
NM_145261.4(DNAJC19):c.210-291del	rs138755965

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