ClinVar Miner

List of variants reported as uncertain significance for autosomal dominant Kenny-Caffey syndrome

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001312909.2(FAM111A):c.1408C>T (p.His470Tyr)
NM_001312909.2(FAM111A):c.1531T>C (p.Tyr511His)	rs587777012
NM_001312909.2(FAM111A):c.1706G>A (p.Arg569His)	rs587777011

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