List of variants in gene DNAJC21 reported as likely pathogenic for not provided

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001012339.3(DNAJC21):c.983+1G>A	rs368148362	0.00002
NM_001012339.3(DNAJC21):c.1155_1156insG (p.Gln386fs)
NM_001012339.3(DNAJC21):c.315+1G>T
NM_001012339.3(DNAJC21):c.439-2A>G
NM_001012339.3(DNAJC21):c.439-32_497del
NM_001012339.3(DNAJC21):c.743+1G>C	rs376653237
NM_001012339.3(DNAJC21):c.895+1G>A

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