ClinVar Miner

List of variants in gene KLHDC8B reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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_173546.3(KLHDC8B):c.722G>A (p.Arg241His)	rs201206162	0.00005
NM_173546.3(KLHDC8B):c.-9G>T	rs2045778895

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