Variants in gene IFT172 with conflicting interpretations "pathogenic" and "likely pathogenic"

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

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HGVS	dbSNP	gnomAD frequency
NM_015662.3(IFT172):c.1525-1G>A	rs370540673	0.00001
NM_015662.3(IFT172):c.4519C>T (p.Arg1507Ter)	rs150246251	0.00001

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