Variants in gene IFT140 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 5

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HGVS	dbSNP
NM_014714.4(IFT140):c.*2G>A	rs144879630
NM_014714.4(IFT140):c.1542C>A (p.Leu514=)	rs141542834
NM_014714.4(IFT140):c.3693G>A (p.Thr1231=)	rs144028766
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=)	rs146172074
NM_014714.4(IFT140):c.3993G>C (p.Gln1331His)	rs35823417

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