ClinVar Miner

List of variants in gene combination CABP4, LOC130006201 reported as uncertain significance for Cone-rod synaptic disorder, congenital nonprogressive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_145200.5(CABP4):c.*1291A>G	rs146149609	0.00124
NM_145200.5(CABP4):c.*1285G>A	rs373857371

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