List of variants in gene DNAJC13 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015268.4(DNAJC13):c.2292-6G>A	rs35575948	0.00927
NM_015268.4(DNAJC13):c.2736G>A (p.Arg912=)	rs61748099	0.00256
NM_015268.4(DNAJC13):c.2708G>A (p.Arg903Lys)
NM_015268.4(DNAJC13):c.4547G>A (p.Arg1516His)
NM_015268.4(DNAJC13):c.5983G>C (p.Val1995Leu)	rs10935014
NM_015268.4(DNAJC13):c.6509T>G (p.Leu2170Trp)

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