List of variants in gene TRPM4 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala)	rs56355369	0.00373
NM_017636.4(TRPM4):c.1575G>A (p.Trp525Ter)	rs71352737	0.00168
NM_017636.4(TRPM4):c.2740A>T (p.Lys914Ter)	rs140799936	0.00094
NM_017636.4(TRPM4):c.3641-17T>G	rs369065473	0.00053
NM_017636.4(TRPM4):c.1242T>C (p.Phe414=)	rs200633475	0.00031
NM_017636.4(TRPM4):c.246G>T (p.Gly82=)	rs756668921	0.00006
NM_017636.4(TRPM4):c.1944C>G (p.Leu648=)	rs1968308985
NM_017636.4(TRPM4):c.2529G>A (p.Gly843=)	rs754769591
NM_017636.4(TRPM4):c.2766C>A (p.Ile922=)	rs774680517
NM_017636.4(TRPM4):c.2778+8del	rs1600513831

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