List of variants in gene KCTD17 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001282684.2(KCTD17):c.486+5G>A	rs201383375	0.00008
NM_001282684.2(KCTD17):c.413G>C (p.Arg138Pro)	rs786205860
NM_001282684.2(KCTD17):c.436G>A (p.Glu146Lys)	rs2517687893
NM_001282684.2(KCTD17):c.517G>A (p.Gly173Ser)	rs1370972985

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