Variants in gene KIF1B with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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	gnomAD frequency
NM_001365951.3(KIF1B):c.2115+6753A>G	rs41274462	0.01960
NM_001365951.3(KIF1B):c.2115+7031T>C	rs149267056	0.00320
NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=)	rs147318592	0.00092
NM_001365951.3(KIF1B):c.2001G>A (p.Leu667=)	rs543345616	0.00006
NM_001365951.3(KIF1B):c.4810G>A (p.Val1604Ile)	rs769092155	0.00004

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