Variants in gene HNF4A with conflicting interpretations "uncertain significance" and "uncertain risk allele"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (uncertain risk allele) minimum review status:		Submission 2 (uncertain risk allele) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_175914.5(HNF4A):c.481A>G (p.Ser161Gly)	rs779555087	0.00001
NM_175914.5(HNF4A):c.101T>A (p.Val34Asp)	rs2063496235

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