ClinVar Miner

List of variants in gene JPH2 reported as uncertain significance for Left ventricular noncompaction cardiomyopathy

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_020433.5(JPH2):c.1540G>A (p.Gly514Ser)	rs869025442	0.00001
NM_020433.5(JPH2):c.1750C>A (p.Gln584Lys)	rs730880253

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