List of variants in gene TRPM4 reported as uncertain significance by Blueprint Genetics

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: 8

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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.1082T>G (p.Leu361Arg)	rs148763371	0.00019
NM_017636.4(TRPM4):c.1069C>T (p.Arg357Trp)	rs764690335	0.00007
NM_017636.4(TRPM4):c.1826C>G (p.Ala609Gly)	rs547541099	0.00006
NM_017636.4(TRPM4):c.3512G>A (p.Arg1171His)	rs762615860	0.00003
NM_017636.4(TRPM4):c.1321G>A (p.Val441Met)	rs587782982	0.00002
NM_017636.4(TRPM4):c.3337C>G (p.Leu1113Val)	rs780954126
NM_017636.4(TRPM4):c.678C>G (p.Asp226Glu)	rs730880236

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