ClinVar Miner

List of variants in gene JUP reported as uncertain significance for Ventricular fibrillation, paroxysmal familial, type 1

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_002230.4(JUP):c.1807G>T (p.Val603Leu)	rs200327969	0.00038
NM_002230.4(JUP):c.2069A>G (p.Asn690Ser)	rs147628503	0.00019

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