ClinVar Miner

List of variants in gene TRPM4 reported as uncertain significance by Division of Human Genetics, Children's Hospital of Philadelphia

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.2674C>T (p.Arg892Cys)	rs147854826	0.00047
NM_017636.4(TRPM4):c.379G>A (p.Gly127Ser)	rs368769982	0.00001

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