ClinVar Miner

List of variants in gene KCTD7 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_153033.5(KCTD7):c.493+18_493+21dup	rs57580125	0.11765
NM_153033.5(KCTD7):c.267G>A (p.Thr89=)	rs3764904	0.08655

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