Variants with conflicting interpretations "uncertain significance" from Fulgent Genetics, Fulgent Genetics and "risk factor" from any submitter

Minimum review status of the submission from Fulgent Genetics, Fulgent Genetics:		Collection method of the submission from Fulgent Genetics, Fulgent Genetics:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_032782.5(HAVCR2):c.245A>G (p.Tyr82Cys)	rs184868814	0.00159
NM_173353.4(TPH2):c.616C>T (p.Pro206Ser)	rs17110563	0.00107
NM_182919.4(TICAM1):c.557C>T (p.Ser186Leu)	rs146550489	0.00063
NM_003265.3(TLR3):c.1660C>T (p.Pro554Ser)	rs121434431	0.00053
NM_020975.6(RET):c.3116C>T (p.Pro1039Leu)	rs79853121	0.00004
NM_020975.6(RET):c.938G>A (p.Arg313Gln)	rs77702891	0.00002

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