Variants in gene GLI3 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000168.6(GLI3):c.1497+1G>A	rs1399654830
NM_000168.6(GLI3):c.1873C>T (p.Arg625Trp)	rs121917712
NM_000168.6(GLI3):c.3640C>T (p.Gln1214Ter)
NM_000168.6(GLI3):c.4431dup (p.Glu1478Ter)	rs1057520063

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