List of variants in gene TRPM1 reported as uncertain significance by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001252024.2(TRPM1):c.3293+5G>A	rs201442201	0.00096
NM_001252024.2(TRPM1):c.281A>G (p.Tyr94Cys)	rs200514769	0.00019
NM_001252024.2(TRPM1):c.362T>C (p.Leu121Pro)	rs191205969	0.00016
NM_001252024.2(TRPM1):c.965G>A (p.Gly322Glu)	rs200374755	0.00010
NM_001252024.2(TRPM1):c.2557T>C (p.Phe853Leu)	rs748304340	0.00006
NM_001252024.2(TRPM1):c.1237A>G (p.Ile413Val)	rs1010630453	0.00005
NM_001252024.2(TRPM1):c.2816G>A (p.Arg939His)	rs779690150	0.00005
NM_001252024.2(TRPM1):c.1604T>C (p.Leu535Pro)	rs777523949	0.00004
NM_001252024.2(TRPM1):c.112C>T (p.His38Tyr)	rs1163630413
NM_001252024.2(TRPM1):c.1572+3G>C
NM_001252024.2(TRPM1):c.2807C>A (p.Ala936Glu)	rs1555419893
NM_001252024.2(TRPM1):c.3763_3764del (p.Asn1255fs)	rs754615589
NM_001252024.2(TRPM1):c.4173_4176del (p.Asp1392fs)	rs767762692

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