ClinVar Miner

Variants in gene HNF4A with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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NM_000457.4(HNF4A):c.1387A>G (p.Ile463Val) rs147638455
NM_000457.4(HNF4A):c.447G>A (p.Leu149=) rs193922473
NM_000457.4(HNF4A):c.505G>A (p.Val169Ile) rs142204928
NM_175914.4(HNF4A):c.224+17dup rs371937621
NM_175914.4(HNF4A):c.726G>A (p.Val242=) rs145280017

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