ClinVar Miner

List of variants in gene TRPM4 reported as uncertain significance for cardiac conduction defect

Included ClinVar conditions (6):

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_017636.4(TRPM4):c.1575G>A (p.Trp525Ter)	rs71352737	0.00168
NM_017636.4(TRPM4):c.1826C>G (p.Ala609Gly)	rs547541099	0.00006

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