List of variants in gene combination LURAP1L, TYRP1 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000550.3(TYRP1):c.1029C>T (p.Asp343=)	rs145061390	0.00089
NM_000550.3(TYRP1):c.1411C>T (p.Arg471Trp)	rs138272660	0.00036
NM_000550.3(TYRP1):c.1138G>T (p.Ala380Ser)	rs184910238	0.00022
NM_000550.3(TYRP1):c.1354A>G (p.Met452Val)	rs761776915	0.00012
NM_000550.3(TYRP1):c.1186A>C (p.Asn396His)	rs765833423	0.00001

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