ClinVar Miner

List of variants in gene DSP reported as uncertain significance for arrhythmogenic right ventricular dysplasia 1

Included ClinVar conditions (2):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.5063C>T (p.Ala1688Val)	rs372288373	0.00005
NM_004415.4(DSP):c.3774C>A (p.Asp1258Glu)	rs748733750	0.00002

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