List of variants in gene DNAJC19 reported as benign for not specified

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_145261.4(DNAJC19):c.285A>C (p.Gly95=)	rs17850540	0.00755
NM_145261.4(DNAJC19):c.69G>A (p.Leu23=)	rs142023670	0.00321
NM_145261.4(DNAJC19):c.281-12T>C	rs141982712	0.00127
NM_145261.4(DNAJC19):c.-29G>T	rs181271620	0.00089
NM_145261.4(DNAJC19):c.210-7T>A	rs779367415	0.00006

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