List of variants in gene DNAJC19 reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_145261.4(DNAJC19):c.331G>C (p.Glu111Gln)	rs370042988	0.00024
NM_145261.4(DNAJC19):c.182G>A (p.Arg61Gln)	rs376891597	0.00016
NM_145261.4(DNAJC19):c.181C>T (p.Arg61Trp)	rs141007488	0.00004
GRCh37/hg19 3q26.33(chr3:180702567-180703988)x1
NM_145261.4(DNAJC19):c.137G>T (p.Ser46Ile)	rs2473930439
NM_145261.4(DNAJC19):c.198dup (p.Leu67fs)	rs2473930224
NM_145261.4(DNAJC19):c.281G>T (p.Gly94Val)	rs151056679

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