ClinVar Miner

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:
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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