ClinVar Miner

List of variants in gene combination HNF4A, R3HDML 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_175914.4(HNF4A):c.-565T>C	rs377144780	0.00051
NM_175914.4(HNF4A):c.-584A>T	rs149135843	0.00020

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