List of variants in gene combination HRC, TRPM4 reported as likely benign for heart conduction disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.1744G>A (p.Gly582Ser)	rs172149856	0.00043
NM_017636.4(TRPM4):c.1294G>A (p.Ala432Thr)	rs201907325	0.00042
NC_000019.10:g.49154455ATC[13]	rs61355957

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