List of variants in gene PRKDC reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006904.7(PRKDC):c.5120T>A (p.Leu1707Gln)	rs202110076	0.00235
NM_006904.7(PRKDC):c.4435G>C (p.Val1479Leu)	rs199731143	0.00104
NM_006904.7(PRKDC):c.7204C>T (p.Leu2402Phe)	rs374403400	0.00051

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