Variants in gene HNF4A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_175914.5(HNF4A):c.340C>T (p.Arg114Trp)	rs137853336	0.00006
NM_175914.5(HNF4A):c.733C>T (p.Arg245Cys)	rs1290868034	0.00001
NM_175914.5(HNF4A):c.200G>A (p.Arg67Gln)	rs1555813319
NM_175914.5(HNF4A):c.2T>C (p.Met1Thr)	rs1229650809
NM_175914.5(HNF4A):c.869G>A (p.Arg290His)	rs1191912908
NM_175914.5(HNF4A):c.931C>T (p.Arg311Cys)	rs193922480
NM_175914.5(HNF4A):c.932G>A (p.Arg311His)	rs1375557127

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